Enjoy Life Natural Brands is expanding its recall of baked goods over the potential presence of pieces of plastic. The items were sold at Trader Joe's grocery stores and online.The original recall, including soft baked cookies and chewy bars, was announced on June 30.Now, one product is being added along with additional "best by" dates on four products.The company said the expanded recall comes from an internal investigation and says it's being done out of an abundance of caution. Below is the full list of recalled items, best by dates marked with * represent additional items in the expanded voluntary recall.Enjoy Life – Soft Baked Cookies – Snickerdoodle, 6 oz with retail UPC 853522000184 and best by dates 2/4/2023, 3/4/2023 and 3/10/2023 Enjoy Life – Soft Baked Cookies – Chocolate Chip, 6 oz with retail UPC 853522000191 and best by dates 2/5/2023, 2/6/2023 and 3/5/2023 Enjoy Life – Soft Baked Cookies – Double Chocolate Brownie, 6 oz with UPC 853522000214 and best by date 3/6/2023Enjoy Life – Soft Baked Cookies – Sunseed Butter Chocolate Chip, 6 oz with retail UPC 819597013801 and best by date 3/3/2023 Enjoy Life – Soft Baked Cookies – Monster, 6 oz with retail UPC 819597013818 and best by dates 2/6/2023 and 3/3/2023 Enjoy Life Chewy Bars – Sunseed Crunch, 5.75 oz with retail UPC 853522000627 and best by date 3/3/2023 Enjoy Life Chewy Bars – Caramel Blondie, 5.75 oz with retail UPC 819597011258 and best by dates 3/3/2023 and 3/4/2023 Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals - Apple Cinnamon, 8.8 oz with retail UPC 819597012569 and best by dates 2/3/2023*, 2/4/2023, 2/12/2023, 2/13/2023, 2/20/2023, 3/12/2023 and 3/13/2023 Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals – Chocolate Chip Banana, 8.8 oz with retail UPC 819597012576 and best by dates 12/31/2022, 1/6/2023, 1/7/2023, 1/19/2023, 1/20/2023 and 2/12/2023 Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals – Berry Medley, 8.8 oz with retail UPC 819597012583 and best by dates 2/3/2023*, 2/10/2023, 2/11/2023 , 2/17/2023  and 3/10/2023 Enjoy Life Brownie Bites – Rich Chocolate, 4.76 oz with retail UPC 819597013290 and best by date 1/10/2023Enjoy Life Brownie Bites – Salted Caramel, 4.76 oz with retail UPC 819597013313 and best by date 1/10/2023Enjoy Life Soft Baked Cookies - Amazon Variety Pack - (2SND,1CC,1OAT,1SBCC,1MSTR) - 6/6 oz with retail UPC 819597014518 and best by dates 9/24/2022 and 1/20/2023 Trader Joe’s Soft Baked Snickerdoodle Cookies, 6 oz. with retail UPC 0094 0757 and best by date 2/3/2023*Click here for more information on the recall from the U.S. Food and Drug Administration. Consumers who have one of the recalled products should not eat it and should discard any product they may have but should keep any available packaging and contact the company at 1-855-543-5335 to get more information about the recall and how to receive a refund.

Approximately 14,400 strollers manufactured by UPPAbaby are being recalled because of a risk of amputating children's fingers.The Consumer Product Safety Commission said in a release that the rear brakes on the brand's All-Terrain Ridge Jogging strollers have "openings that can cause amputation or laceration if a non-occupant child's fingertip gets caught in the openings while the stroller is in use."The agency said it has received one reported incident in which a child, who wasn't in the stroller, had their fingertip amputated. The $600 stroller has been sold at a number of retailers, including Amazon, BuyBuyBaby, Nordstrom, Neiman Marcus and Pottery Barn Kids.The problematic strollers have serial numbers that begin with "1401RDGUS" on the stroller's right side above the rear wheel. The strollers have a black frame and were sold with three fabric colors, including white, charcoal and slate blue.Affected consumers should stop using the strollers and contact UPPAbaby for free replacement brake discs for both wheels.UPPAbaby didn't immediately respond to CNN Business' request for comment.

The Seed Ranch Flavor Co. is recalling several products sold on Amazon.com and at a handful of retailers as the products contain undeclared soy.

The recalled products include 5 fl ounce bottles of "Umami Everyday Sauce" and “Everything But The Sushi & Dumplings” sauce.

The Food and Drug Administration said, “People who have allergies to soy run the risk of serious or life-threatening allergic reaction if they consume these products.”

No one has reported becoming ill from the products.

“The recall was initiated after it was discovered that the soy-containing product was distributed in packaging that did not explicitly reveal the presence of soy. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes during a label redesign,” the FDA said.

Those who have recalled products are encouraged to discard or return them.

The FDA lists the affected lot numbers on its website.

Honda is recalling nearly 1.2 million vehicles in the U.S. because the rear view camera image may not appear on the dashboard screen.The recall covers certain Odyssey minivans from 2018 to 2023, as well as Pilot SUVs from 2019 to 2022 and Passport SUVs from 2019 to 2023.Honda says in documents posted Friday by U.S. safety regulators that the problem was traced to a faulty coaxial cable connector. The National Highway Traffic Safety Administration says if the rear view camera image doesn't display, it can cut driver visibility and increase the risk of a crash.The company says it received nearly 274,000 warranty claims from May of 2017 through June 8. It has no reports of any injuries.Dealers will replace a cable harness and install a straightening cover at no cost to owners, who will be notified by letter starting July 24.

Subaru has advised owners of certain SUVs to park them outside after they've recalled more than 271,000 SUVs due to a potential fire risk.

According to a National Highway Traffic Safety Administration report, the recall affects 2019-22 Ascents.

The recall was issued due to the possibility of a ground bolt improperly fastened that connects the ground terminal of the Positive Temperature Coefficient (PTC) heater, the report stated.

The company said this could cause the ground terminal and surrounding components to melt, according to the recall notice.

The NHTSA said the car company has advised owners to park the affected vehicles outside and away from structures.

They are also advised not to leave them unattended if the engine is running, according to the agency's report.

According to the notice, if drivers see or smell smoke coming from the dashboard or the driver's footwell area, they should immediately stop driving the vehicle and turn the ignition off.

Subaru said owners should take their cars to a dealership where the problem can be fixed for free.

The company added that owner notification letters should be mailed beginning Feb. 6.

The U.S. Consumer Product Safety Commission (CPSC) and Target are announcing the recall of about 204,000 Pillowfort Weighted Blankets due to an asphyxiation hazard, which has caused two fatalities. A 4-year-old girl and a 6-year-old girl reportedly became entrapped in the cover of the weighted blanket and died due to asphyxia at Camp Lejeune, North Carolina, in April 2022. Target has received four reports of children becoming entrapped in these weighted blankets, including the two fatalities.CPSC and Target, which is based in Minnesota, are urging consumers to stop using the recalled weighted blankets immediately and contact Target for a refund. The blankets weigh 6 pounds, measure 60 inches long and 40 inches wide and have a removable, waterproof, washable cover. The blankets come in eight prints or colors including unicorn white, space navy, pink, blue, gray, buffalo plaid red, blue constellation, and unicorn pink. Item numbers 097-02-0140 (Unicorn - White), 097-02-0148 (Space Navy), 097-02-0361(Pink), 097-02-0363 (Blue), 097-02-0364 (Gray), 097-02-1603 (Buffalo Plaid – Red), 097-02-3904 (Blue Constellation) and 097-02-3905 (Unicorn – Pink) are printed on the fabric tag attached to the removable covers of the blankets.The weighted blankets were manufactured in China.Target exclusively sold the recalled weighted blankets at Target stores nationwide and online at www.target.com. The blankets were sold from December 2018 through September 2022 for $40. Contact Target at 800-440-0680 from 7 a.m. to 10 p.m. CT daily to receive a prepaid return label to return the blankets by mail or return to any Target store. Go online at www.target.com and click on "Recall Information," then on "Home Goods," for more information. Target is also contacting all known purchasers directly to arrange returns.The consumer will receive a refund of $40 in the form of a credit for use at Target stores or online at www.target.com, or the amount on the purchase receipt if higher. Consumers can also click the "Products Recalls" tab on Target’s Facebook page for more information.

Ford is recalling nearly 400,000 vehicles because their 360-degree camera may not work properly.

The recall involves 2020-2023 Explorers, Lincoln Aviators and 2020-2022 Lincoln Corsairs.

Ford says the video output on the camera may fail, preventing the rearview camera image from displaying.

"Loss of the rearview camera image can reduce the driver's rear visibility, increasing the risk of a crash," Ford notes.

The automaker says it's aware of 17 reported minor accidents that may be related to the faulty video output, which causes a blue screen. No injuries have been reported.

Owners should receive letters in February to take their vehicles in to be serviced. Dealers will update the necessary software for free, Ford states.

Banana Boat is expanding its recall of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 due to the presence of benzene, which is classified as a human carcinogen.

Edgewell Personal Care Company says an additional batch of the sunscreen was added to the recall announcement from July.

The products all feature the same UPC code: 0-79656-04041-8. However, they have different lot codes and expiration dates.

Lot Code Expiration Date 
20016AF Dec. 2022
20084BF Feb. 2023
21139AF April 2024
20301CF Sept. 2023

The company says the sunscreen was distributed nationwide and sold at various retailers and online. It adds that it has notified retailers to pull the product from their shelves.

Benzene is not an ingredient in Bobana Boat products, according to Edgewell Personal Care Company. However, the company says "a review showed that unexpected levels of benzene came from the propellant that sprays the product out of the can."

The Centers for Disease Control notes that benzene can be found in the environment due to a variety of factors, including tobacco smoke, vehicle exhaust and industrial emissions.

The agency warns that long-term exposure to benzene can affect the immune system and cause cancer.

Consumers are asked to discard the recalled sunscreen. They can contact Edgewell Personal Care at 1-888-686-3988 for information about how to be reimbursed.

Parents – check your pantries for baby formula.

Reckitt announced on Sunday that it was voluntarily recalling two select batches of ProSobee 12.9 oz.

In a press release, it was noted that Simply Plant-Based Infant Formula is being recalled out of an abundance of caution due to "a possibility of cross-contamination with Cronobacter sakazakii. All product distributed went through extensive testing and tested negative for the bacteria."

The product, which was distributed nationwide in retail stores in the U.S., Guam and Puerto Rico, was manufactured between August and September 2022.

You can identify these batches of formula by a number that is found on the bottom of the can.

"Recalled product batches are ZL2HZF and ZL2HZZ both with a UPC Code of 300871214415 and a “Use By Date” of “1 Mar 2024," the press release stated.

Approximately 145,000 cans of the formula are impacted by the recall.

Reckitt says no other products are impacted and no illnesses have been reported.

"The batches in question tested negative for Cronobacter and other bacteria and this is an isolated situation. After a thorough investigation, we have identified the root cause, which was linked to a material from a third party. We have taken all appropriate corrective actions, including no longer sourcing this material from the supplier."

If you bought the ProSobee Simply Plant-Based Formula in question, check the can to identify if it's from an affected batch. You can also contact the company at consumer.relations@rb.com for assistance.

For more information, click here.

Approximately two million air fryers have been recalled due to concerns that a wire connection can overheat, posing fire and burn hazards. According to a recall notice from the U.S. Consumer Product Safety Commission, there have been more than 200 reports of Cosori air fryers catching fire, burning, melting, overheating and smoking. These include 10 reports of minor, superficial burn injuries and 23 reports of minor property damage.The recall notice includes Cosori air fryers with the following model numbers: CP158-AF, CP158-AF-R19, CP158-AF-RXW, CP158-AF-RXR, CAF-P581-BUSR, CAF-P581-AUSR, CAF-P581-RUSR, CP137-AF, CP137-AF-RXB, CP137-AF-RXR, CP137-AF-RXW, CS158-AF, CS158-AF-RXB, CS158-AF-R19, CAF-P581S-BUSR, CAF-P581S-RUSR, CAF-P581S-AUSR, CO137-AF, CO158-AF, CO158-AF-RXB and CP258-AF. Model numbers are printed on the bottom label of each unit and on the accompanying user manual. The recalled units are the 3.7-quart and 5.8-quart sizes sold in black, gray, white, blue and red colors.The air fryers included in the recall were sold at Best Buy, Target and Home Depot stores nationwide and online through Amazon, Adorama, Bed Bath & Beyond, Cosori, eBay, Home Goods, Kohl's, Lowes, Macy's, QVC, Staples, Vesync, Walmart, Wayfair, Wellbots and Woot from June 2018 through December 2022 for between $70 and $130.If you own one of the air fryers involved in the recall, stop using it immediately and contact Consori for a free replacement air fryer or another Cosori product by registering at recall.cosori.com. Registration requires customers to provide contact information and photos of the recalled unit with the cord cut off. No receipt is required to receive a replacement.

DETROIT —

Jaguar is recalling more than 6,000 I-Pace electric SUVs in the U.S. due to the risk of the high-voltage battery catching fire, and it's telling owners to park them outdoors.

The recall is the latest in a series of electric vehicle battery recalls because of the potential for fires.

Documents posted Wednesday by the U.S. National Highway Traffic Safety Administration say the recall covers all of the SUVs from the 2019 through 2024 model years.

In an email, Jaguar said customers should park away from structures until recall repairs have been completed, and where possible, they should charge outdoors. Owners with questions should contact a dealer if they have any concerns, the company said.

The documents say the vehicle batteries were made by LG Energy Solution, which is under investigation by the NHTSA after five automakers issued recalls due to possible defects that could cause fires or stalling.

The NHTSA opened the probe in April of 2022 covering more than 138,000 vehicles with the South Korean company's lithium-ion batteries.

General Motors, Mercedes-Benz, Hyundai, Stellantis and Volkswagen have issued recalls since February of 2020, most due to internal battery failures that can increase the risk of fires.

The agency said it will write to LG and other companies that might have bought similar batteries to make sure recalls are being done when needed.

LG Energy Solution, based in Seoul, South Korea, noted that Jaguar is updating the battery-managing software on the vehicles while the incidents that led to the recall are being investigated.

"LG Energy Solution continues to closely work with our client Jaguar Land Rover to ensure that the investigation is concluded," it said in a statement Thursday.

The investigation is another bug in a growing global rollout of electric vehicles by all automakers to replace internal combustion vehicles to cut emissions and fight climate change. Ford and BMW also have recalled batteries in recent years. Also, the U.S. National Transportation Safety Board investigated a series of fires in Tesla vehicles and said the high-voltage lithium-ion batteries pose safety risks to first responders after crashes.

Many governments are counting on EVs to replace gasoline-burning vehicles that emit greenhouse gases that cause global warming.

Documents in the Jaguar recall say the battery energy control module software will be updated by a dealer or online. The dealers also will replace battery modules if needed.

The documents say that Jaguar has received eight reports of vehicle fires in the U.S. starting in June of 2019.

CNN —

A rare strain of bacteria found in recalled eye drops has been linked to dozens of infections, as well as cases of vision loss and surgical removal of eyes. This week, the U.S. Centers for Disease Control and Prevention reported two additional deaths — a total of three — have been linked to the bacterial infection.

Video above: An infectious disease doctor discusses the drug-resistant bacteria found in eye drops.

Global Pharma Healthcare recalled its Artificial Tears Lubricant Eye Drops that were distributed by EzriCare and Delsam Pharma last month, and the agency has been warning people not to use the drops.

As of March 21, the CDC has identified 68 people in 16 states with infections of a rare strain of drug-resistant Pseudomonas aeruginosa never before reported in the United States. Most of the patients reported using artificial tears, the CDC said, and EzriCare Artificial Tears was the brand most commonly reported.

Reported adverse events include infections of the cornea, bloodstream, respiratory tract and urinary tract. There are eight reports of lost vision and four reports of surgically removed eyeballs.

On Wednesday, two case reports published in JAMA Ophthalmology offered more details about how these problems developed

One of the new case reports described a 72-year-old woman who lost vision in her left eye after using EzriCare artificial tears for dry eyes for about a week.

"She started noticing some blurry vision in her left eye for a few days," said Dr. Ahmed Omar, an ophthalmologist at University Hospitals Cleveland Medical Center, who treated the woman. "It was initially painless, but according to the patient and her husband, one morning she woke up and she had a yellow discharge on her pillow. And that's when she started noticing that the appearance of her eye had changed."

The woman went to the emergency room, where doctors discovered a large ulcer on her left cornea, nearly involving the entire eye. She was admitted to the hospital for three weeks, requiring IV antibiotics, antibiotic eye drops, and multiple surgical interventions.

The woman's case was complicated by a serous choroidal detachment, an abnormal accumulation of fluid, which ultimately led to vision loss in the left eye.

Another case involved a 72-year-old man who developed multidrug-resistant Pseudomonas aeruginosa keratitis, an infection of the cornea.

The man went to the Bascom Palmer Eye Institute in Miami after a day of severe pain and decreased vision in his right eye. He had no previous eye problems but said he had used EzriCare artificial tears for eye dryness.

"When we examined his right eye, there was a severe corneal infection," said Dr. Marissa Shoji, a resident physician at the institute, who treated the patient. "He could only see shadows and was not able to see letters due to the extent of the ulcer."

The man was started on strong antibiotics, Dr. Naomi Gutkind, a resident physician who also treated him, said.

"We typically expect some degree of improvement these medications, but when we saw him two day later, he was getting far worse," she said. "So that's when we inquired about specifically the EzriCare tears, because we knew they were associated with resistant infection that may not respond to those really strong antibiotics."

Cultures from the man's cornea and EzriCare bottle grew the same strain of multidrug-resistant Pseudomonas.

The man's vision at his two months follow-up appointment was 20/400, meaning he can see at 20 feet what healthy people can see at 400 feet.

"At some point, he was in danger of having permanent vision loss," said Dr. Guillermo Amescua, an ophthalmologist at Bascom Palmer Eye Institute. "He now has what is called corneal blindness because he's 20/400 and has a corneal scar, but with corneal transplantation, he might have a better prognosis."

Shoji says this case highlights the short-term and long-term effects of Pseudomonas keratitis. In the short term, people may have terrible pain, decreased vision and a risk of a hole in the eye that could spread infection.

"In the long term, even after the infection is cleared, there's a risk of needing a surgery such as a corneal transplant or other different types of surgeries to address scarring that may also significantly limit the vision," she said.

What to know about infections

EzriCare said in a statement that after learning about the CDC's investigation of Pseudomonas infections on Jan. 20, it "immediately took action to stop any further distribution or sale of EzriCare Artificial Tears. To the greatest extent possible, we have been contacting customers to advise them against continued use of the product."

The physicians involved in the new studies hope that by highlighting these cases, they can spare others from similar problems.

Shoji advises against using EzriCare or Delsam eye drops while the investigation is ongoing.

"If you have any eye symptoms, things like eye pain, eye redness, decreased vision, please see an ophthalmologist for evaluation," she said. "And when you come, please bring anything that could potentially be causing this infection, especially eye drops, contact lenses or contact lens cases."

The CDC says symptoms can include yellow, green or clear discharge from the eye; eye pain or discomfort; redness of the eye or eyelid; feeling like something is in the eye; increased light sensitivity; and blurry vision.

Doctors urge everyone to use caution with eye drops.

"I think a lot of times, people don't think of eye drops or even things like contact lenses as medical devices. I think they think of them more as kind of just an over-the-counter product like a skin lotion or something like that," said Dr. Christina Prescott, a NYU ophthalmologist who wrote a commentary published alongiside the case reports on the potential rare dangers of presumably benign artificial tears.

Prescott says people should keep eye drops sterile. That means avoiding touching the tip of the bottle with their hands, skin or eye; not sharing the bottle with someone else; and not using expired products.

People should also use caution with preservative-free eye drops because contamination can lead to serious infection.

"Anything you're putting in your eye, if it's contaminated, is going to have a high risk of infection just because your eyes are so vulnerable," she said.

Related video above: How to check if your rental is safe

Volkswagen is recalling 143,000 of its big Atlas SUVs in the U.S. because a faulty sensor on the front passenger side can switch the airbag system off under certain conditions. Until the issue can be corrected, VW is advising owners to avoid letting people ride in that seat.

The problem is "sporadic," according to documents VW filed with the National Highway Traffic Safety Administration, which oversees vehicle recalls.

Most modern passenger vehicles have weight sensors in the front seat to detect if someone small -- like a child -- is riding in that seat. Airbags, which inflate forcefully in the event of a crash, can injure small children. If these sensors detect a small person is seated there, the airbag is switched off.

But faulty sensors in some Atlas SUVs can cause the so-called "passenger occupant detection system" to indicate a system issue and deactivate the airbag. This could leave front-seat passengers without the protection of the airbag in the event of a crash.

While it's still unclear what's causing the problem, VW investigators were able to determine that it was happening in Atlases built during two specific time periods. The vehicles being recalled are all model year 2018 through 2021 Atlas and model year 2020 Atlas Cross Sport SUVs.

Volkswagen is unaware of any injuries that might have resulted from the problem, VW spokesman Mark GIllies said.

If this problem occurs, a warning light will illuminate inside the vehicle. VW hasn't determined how to fix the problem yet but, once that's figured out, repairs will be done free of charge, according to documents VW filed with NHTSA. Owners of recalled Atlas SUVs will be notified by mail.

Concerned owners can also call NHTSA's auto safety hotline at 1-888-327-4236.

The Atlas, a seven-seat SUV that was designed specifically for the US market, is built at VW's Chattanooga, Tennessee, factory.

The U.S. Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines.

Related video above: Sleep apnea sufferers troubled by CPAPs could try new treatment

A Class I recall means the FDA has determined a reasonable probability that a product could "cause serious adverse health consequences or death."

"Philips is recalling certain reworked Philips DreamStations because some devices were assigned incorrect or duplicate serial numbers during initial programming," the recall notice says. "This duplication can cause therapy to be delivered using the wrong prescription or factory default settings. Additionally, it may fail to deliver any therapy at all. There is no warning or indication to the user that the DreamStation is not working the way the doctor intended or prescribed."

The problem could lead to serious health problems such as heart failure, respiratory failure or death, the FDA says.

Phillips has received 43 complaints about the issue, but there have been no reported injuries or deaths.

These machines help with certain breathing conditions that don't allow people to breathe in a regular rhythm. The machines provide continuous positive airway pressure, known as CPAP, to keep the airways open with a steady stream of air through a mask or bilevel positive airway pressure, also known as BiPAP support, pumping air into the lungs using different pressures.

People who have sleep apnea or obstructive sleep apnea, potentially serious disorders in which they may stop breathing at night, can use these machines to keep their airways open during sleep.

The recall involves 1,088 machines distributed from Dec. 1, 2021, to Oct. 31, 2022.

Philips has sent letters to affected customers to encourage them to continue to use the devices until a replacement is sent or their health care provider makes pressure changes on their current device.

The fastest way to manage the problem, the FDA says, is to contact the provider to ask about a manual reset of pressure, either remotely or in person.

For further details, call 1-877-387-3311, email patientsupport@philips.com or visit Philips' website.

The U.S. Food and Drug Administration issued a warning on Friday to consumers and health providers to discontinue using and discard recalled Pilot COVID-19 at-home tests made by SD Biosensor, Inc. over "significant concerns" of bacterial contamination.

SD Biosensor is recalling all impacted tests, which were distributed by Roche Diagnostics to various retailers to stop the spread of COVID-19 infections.

Throw out any Pilot tests from the affected lot numbers and do not pour the liquid solution down the drain, the FDA said.

"Direct contact with the contaminated liquid solution may pose safety concerns and the bacterial contamination could impact the performance of the test," the FDA said in a news release.

The FDA said the tests may be contaminated with bacteria such as enterococcus, enterobacter, klebsiella and serratia species and cause infection. Bacterial infections may cause illness in people with weakened immune systems.

If the liquid comes into contact with skin or eyes, flush with large amounts of water and get medical attention if irritation persists. Signs and symptoms of bacterial infection can include fever, discharge, or red eyes.

Some 500,000 tests were distributed to CVS Health, as well as about 16,000 tests to Amazon, the FDA said, and the agency is working with Roche Diagnostics to determine how many tests were sold to consumers.

The FDA notes that none of the impacted lots were distributed through any federal testing programs.

"If you received your tests through the COVID.gov/tests distribution or as part of other federal testing programs, they are not subject to this safety communication or product recall," the release said.

A beach chair sold at Family Dollar is being recalled amid consumer reports of it collapsing unexpectedly.

According to the U.S. Consumer Product Safety Commission, about 38,000 of the Beach Loungers were recalled because they pose a risk of injuring if fingers get caught in the metal folding joints.

No injuries have been reported.

The agency said the chairs have a tag on one side that says Outdoors by Design on one side and Distributed by Midwoods Brands LLC on the other.

If you own this product, you are asked to stop using it immediately and return it to a Family Dollar store for a full refund.

An Oklahoma woman is still waiting for a life-saving machine after the U.S. Food and Drug Administration recalled millions of the device.

One of the largest manufacturers of machines that help people with sleep apnea has been recalled. An FDA investigation found that some of the machines were potentially releasing cancer-causing particles or chemicals.

The recall started back in June, but those who are dependent on these lifesaving devices are still waiting for their replacement.

Dr. Juanita Johnson has been waiting for over a month for a CPAP machine. She has relied on her machine to sleep safely after she suffered a stroke back in 2018.

"It's extremely important. I don't think I would have survived if it were not for the CPAP," Johnson said.

However, for the past month, she has been without the machine. She has had to sleep upright since her CPAP machine went up in smoke.

"I was asleep and I woke up cause I could smell something. My CPAP machine was smoking," Johnson said.

She has been trying to replace it ever since, but she can’t find one anywhere.

"When I called the place that I got it, the insurance paid for it, they told me there was a shortage and they didn't know when they'd be able to get another one," Johnson said.

Some medical supply companies have said the massive recall has left their shelves empty.

"Yeah, we're still waiting. I mean, the last CPAP we had here was probably, oh gosh, a couple months ago?" said Connor Reyburn, a sales associate at Lindsey Medical Supply in Edmond, Oklahoma.

Philips Respironics had to recall 34 million CPAP, BIPAP and other ventilators after the FDA found the foam used to reduce sound and vibration in the devices could degrade and enter the air pathway, which could potentially leave people to breathe in life-threatening foam particles or chemicals.

Philips is in the repair process, but now millions with sleep apnea are left waiting and sleeping in fear.

"I think that may be why I don't sleep well. I get concerned about- they find people dead, ya know? I know it's serious," Johnson said.

Philips expects the repair process to take a year, hopefully wrapping up this September.

Johnson received some good news, though, and her new CPAP machine is expected to be delivered Friday.

You can see if your device is part of the recall here or here.

Watch the video above for the full story.

Sun Valley Foods is recalling ready-to-eat beef and chicken taquitos and chimichangas products containing diced green chilies due to concerns that the products may be contaminated with extraneous materials, specifically hard plastic.

The hard plastic may pose a choking hazard or cause damage to teeth or gums.

The frozen RTE meat and poultry taquitos and chimichangas items were produced by Ajinomoto Foods North America, Inc., and are sold under brand names including Great Value, Casa Mamita and José Olé.

The FDA said the following products, sold nationwide, were recalled:

• 19.2-oz. carton containing 16 pieces labeled as “Great Value Flour Chicken Taquitos Tortillas Stuffed with All White Chicken Meat & Monterey Jack Cheese” with a best if used by date of “11 JUL 2021” and “P5590” printed on the side panel.
• 20-oz carton containing 20 pieces labeled as “CASA MAMITA BEEF TAQUITOS ROLLED IN CORN TORTILLAS” with a best by date of “26 JUN 2021” and “EST 5590” printed on the side panel.
• 22.5-oz carton containing 15 pieces labeled as “CASA MAMITA CHICKEN AND CHEESE TAQUITOS ROLLED IN FLOUR TORTILLAS” with a best by date of “26 JUN 2021” and “P5590” printed on the side panel
• 15-oz. carton containing 15 taquitos labeled as “JOSÉ OLÉ TAQUITOS CHICKEN AND CHEESE POLLO Y QUESO IN FLOUR TORTILLAS” with a best by date of “08 JUL 2021” or “18 JUL 2021,” and “P5590” printed on the side panel.
• 20-oz. carton containing 20 taquitos labeled as “JOSÉ OLÉ TAQUITOS BEEF CARNE DE RES IN CORN TORTILLAS” with a best by date of “08 JUL 2021” and “EST 5590” printed on the side panel.
• 22.5-oz carton containing 15 taquitos labeled as “JOSÉ OLÉ TAQUITOS CHICKEN AND CHEESE POLLO Y QUESO IN FLOUR TORTILLAS” with a best by date of “09 JUL 2021,” “14 JUL 2021” or “17 JUL 2021” and “P5590” printed on the side panel.
• 55.5-oz carton containing 37 taquitos labeled as “JOSÉ OLÉ VALUE PACK TAQUITOS CHICKEN AND CHEESE POLLO Y QUESO IN FLOUR TORTILLAS” with a best if used by date of “15 JUL 2021” and “P5590” printed on the side panel.
• 60-oz. carton containing 60 taquitos labeled as “JOSÉ OLÉ TAQUITOS BEEF CARNE DE RES IN CORN TORTILLAS” with a best if used by date of “9 JUL 2021” or “10 JUL 2021,” and “EST 5590” printed on the side panel.
• 5-oz. individual plastic bag containing “JOSÉ OLÉ CHIMICHANGAS LOADED BEEF NACHO” with a best by date of “15 JUL 2021” and “EST. 17417” printed on the label.

The products bear the establishment number “EST 5590,” “P5590” or “EST. 17417” printed on the packaging above the expiration date.

Ajinomoto Foods North America, Inc. identified pieces of hard plastic in their production process and in a barrel of diced green chilies that was received from their ingredients supplier, Sun Valley Foods. Sun Valley Foods initiated a recall of the green chilies with the FDA.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

To learn more about the recall, click here.

This story was originally published by staff at WTKR.

Butterball is recalling 14,107 pounds of ground turkey products that could be contaminated with blue plastic, according to a news release from the U.S. Department of Agriculture's Food Safety and Inspection Service.

The ground turkey items included in the recall were produced on Sept. 28. The products include 2.5-pound trays containing "Farm to Family Butterball all natural ground turkey" with the case code 50211271, a sell or freeze by date of Oct. 18 and timestamps from 2123 through 2302 on the packaging.

Also included in the recall are 3-pound trays containing Kroger ground turkey with the case code 50211271, a sell or freeze by date of Oct. 17 and timestamps from 2314 through 2351 on the packaging.

The recalled items were shipped to retailers nationwide.

According to the USDA news release, customers reported pieces of blue plastic embedded in raw ground turkey to Butterball and the USDA's inspection service.

There have been no confirmed reports of injuries due to consumption of the recalled products.

USDA officials are concerned that consumers may have some of the recalled products in their refrigerators or freezers. Anyone who purchased the products should not consume them. The USDA recommends throwing them away or returning them to the place of purchase.

Consumer questions about the recall can be directed to the Butterball Consumer Hotline at (800) 288-8372.

The U.S. Food and Drug Administration has announced a recall of several pet food products after more than two dozen dogs have died and several were sickened after eating them.

According to the FDA announcement, several Sportmix pet food products manufactured by Midwestern Pet Foods, Inc. may contain potentially fatal amounts of aflatoxin.

The FDA is aware of at least 28 deaths and eight illnesses in dogs that ate the recalled products and an investigation is ongoing.

Multiple product samples were tested by the Missouri Department of Agriculture and found to contain very high levels of aflatoxin, the FDA said in its news release.

The recall includes several types and sizes of Sportmix pet foods that were distributed nationally in stores and online.

FDA and the Missouri Department of Agriculture are working with the firm to determine whether any additional products will be added to the recall.

Aflatoxin is produced by a mold that can grow on corn or other grains used in pet foods. High levels of aflatoxin can cause illness and death in pets.

According to the FDA, pets with aflatoxin poisoning may have the following symptoms: sluggishness, loss of appetite, vomiting, jaundice (yellowish tint to the eyes or gums due to liver damage), and/or diarrhea.

The FDA is encouraging pet owners to stop feeding their pets the recalled products and consult a veterinarian, especially if their pet is showing signs of illness.

The agency is also asking veterinarians who treat aflatoxin poisoning to report cases. Pet owners can also report suspected cases.

For a full list of products in the recall and more information, click here.

Those Hot Pockets in your freezer could contain something more dangerous than piping hot cheese.

Nestlé Prepared Foods is recalling certain pepperoni Hot Pockets over concerns they may be contaminated with pieces of glass and hard plastic, the U.S. Department of Agriculture's Food Safety and Inspection Service announced Friday.

The Class I recall applies to 54-ounce 12 packs of pepperoni Hot Pockets with a best by date of February 2022 and lot codes 0318544624, 0319544614, 0320544614, and 0321544614. The establishment number "EST. 7721A" appears inside the USDA mark of inspection on the packaging.

A Class I recall involves a "health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death," according to the USDA website.

Approximately 762,615 pounds of the recalled Hot Pockets were shipped to stores across the country.

There are four consumer complaints of extraneous materials inside the Hot Pockets, the Food Safety and Inspection Service said.

One of the complaints includes a report of a minor oral injury, officials said.

Consumers who purchased the recalled product should throw it away or return it to the place of purchase, the Food Safety and Inspection Service said.

Millions of people rely on machines to help them with sleep disorders, but now some of the devices have been recalled because they could pose serious health problems.

Baltimore sister station WBAL-TV reported many people are having difficulties getting replacements, and what a Maryland man did to protect his health.

Charles Mercer believes his machine helped change his life.

"My wife always complained about me snoring, and then she said, 'You know, you actually stop breathing at night,'" Mercer said.

Mercer suffers from sleep apnea, and the device he uses is designed to keep him breathing without any pauses while he sleeps. Mercer has had it for less than a year, and now he worries it could cause him harm.

"I could see if I had broken it or misused it — none of that. It was working fine," Mercer said.

Mercer stopped using his DreamStation in June after Philips, the manufacturer, announced a voluntary recall of certain continuous positive airway pressure (CPAP), bilevel positive airway pressure (BiPap) and ventilator machines.

WBAL checked with Northwest Hospital and other places that help patients who have sleep disorders.

"It's very scary. We have a lot of patients concerned. We hear about it from patients who come to our sleep labs," said Sarah Tencza, with respiratory and sleep services at Northwest Hospital.

Philips lists the recalled machines on its website and explains the foam used to reduce sound and vibration may break down.

According to the U.S. Food and Drug Administration, black debris from the foam or certain chemicals released into the device's air pathway may be inhaled or swallowed. Nationwide, the FDA said there have been more than 1,200 complaints and more than 100 injuries reported.

Exposure to the debris or chemicals could cause health issues, including skin, eye and respiratory irritation; headaches; asthma; nausea; and it could also impact the kidneys, liver or potentially cause cancer, according to the FDA.

"Normally, when things break, you have a recall and the company fixes it just like a car," Mercer said.

But the company said it has no quick fix.

In an email, Mario Fante, senior press officer for the Philips Global Press Office, wrote: "We fully understand the impact this is having on patients. Our priority is to replace the foam in all affected devices either by repair or replacement. We are unable to provide an immediate solution at this time."

Philips estimates 3 million to 4 million units are in use globally — about half of which are in the United States. The company said it has "increased production of repair kits and replacement devices" to 55,000 a week and hopes to increase that capacity to 80,000.

But the company can't send them out yet. It's still waiting for regulatory clearance from the FDA.

Meanwhile, Philips advises against using the affected CPAP and BiPap machines and suggests users consulting their doctor.

Dr. Jennifer So, the University of Maryland Sleep Lab's director, said patients definitely need to talk to their physicians about their best options "to see if the small risks from foam degrading and not using the machine is greater than the benefits they may get from being able to sleep and breathe at nighttime and maintain oxygen saturation."

So said in some cases, not using the machines can lead to uncontrolled blood pressure and heart and lung problems.

"I'm scared to use this one. They said, 'Use it if you want at your own risk.' I said, 'I don't know about that,'" Mercer said.

Mercer said he did register his BiPap machine online as Philips requested. When he stopped using his DreamStation, his wife didn't like it.

"I started going back to snoring. She was complaining. I said, 'I got to do something,'" Mercer said, laughing.

To keep peace at home and protect his health, Mercer purchased a different machine from another company. Others have done the same, and that has caused a shortage of sleep apnea machines. Mercer now wonders if he'll get reimbursed the more than $1,700 he spent on the replacement.

"Sometimes, you look for justice. Sometimes, there is none. You just have to keep surviving," Mercer said.

Philips claimed using what's called an inline bacterial filter may help. Mercer didn't have much confidence in that solution. The FDA said it has no evidence of the safety or effectiveness of using that type of filter for mitigating foam risks.

Philips said people who use an affected ventilator should not stop using it and should consult their doctor.

Ford Motor Company is recalling more than 150,000 vehicles for safety concerns related to airbags after losing track of some of the "obsolete" pieces.

In a notice posted this week, the company says some vehicles “may have had obsolete Takata service parts installed in collision and theft repairs after the Takata recall was completed.”

The company said a few dozen recalled pieces could not be located when the service part was purged, and they are recalling about 154,000 vehicles that may have had them installed during a repair.

“Following extensive investigation and tracing, Ford could not account for some of the obsolete Takata service parts, indicating they may have been installed on vehicles as part of collision or theft repairs,” the statement reads. They also said they were issuing the recall at the request of the U.S. National Highway Traffic Safety Administration.

This recall includes about 153,000 Rangers from 2004 to 2006.

Another recall, also over concerns about obsolete Takata air bag parts, includes about 1,100 vehicles. These include certain Rangers, Mustangs, GTs, Fusions and Edges from 2004 to 2012.

More details and specific recalled vehicles can be found on Ford’s website.

McCormick is voluntarily recalling three spices over concern of salmonella contamination.

The three spices are Perfect Pinch Italian Seasoning, Culinary Italian Seasoning and Frank's RedHot Buffalo Ranch Seasoning.

McCormick shipped the spices to 32 states. So far, no illnesses have been reported.

Consumers are urged to dispose of the recalled product and its container.

Please contact McCormick Consumer Affairs at 800-635-2867 from 9:30 a.m. to 8 p.m. ET on weekdays for a replacement or full refund, and with general inquires.

For affected date codes and other product information, click here.