794 recalls tagged with “infant product”.
Anna Queen recalls Play Yards sold on Amazon due to suffocation and entrapment risks. The product features black fabric sides, gray mesh panels, and white top rails with a bear-print design. Model P700 and production date 202503 appear on packaging and a removable tag. Consumers should stop using recalled units and obtain a full refund from Anna Queen.
Anzmtosn recalled 15-piece Magnet Fidget Spinner Sets sold on Amazon after magnets pose a serious ingestion hazard. The magnets can detach and, if swallowed, attract each other or metal objects and cause internal injuries. Stop using the sets now and email disposal photos to Anzmtosn53@163.com for a full refund.
Mallimoda recalled its children’s pajama sets sold on Amazon due to a burn hazard risk. The recall cites violations of mandatory sleepwear standards. Consumers should stop using the recalled sets and contact Mallimoda for a full refund.
Little Partners recalled its Grow 'N Stow Folding Learning Tower after a platform collapse could cause a child to fall. The recall covers LP01711 units with date codes 202409 through 202501. Consumers should stop using the recalled tower immediately and contact Little Partners for a free repair kit.
Bearlala baby loungers sold on Walmart.com by Nuoxuann are recalled. The recall cites a violation of the mandatory Infant Sleep Products standard. The loungers have sides that are too low and foot openings that are wider than allowed, creating fall and entrapment hazards. Consumers should stop using the loungers immediately and contact Nuoxuann for a full refund.
AliExpress recalls a convertible stroller sold online from September 2024 through October 2025 for $215 to $415. The restraint system can fail, creating a fall hazard that could cause serious injury or death. Stop using the stroller now and contact AliExpress for a full refund; you must cut the restraints and email a photo of the destroyed product.
Romorgniz recalled fabric 12- and 13-drawer dressers sold on Amazon after reports of tip-over and entrapment hazards. The units violate the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and contact Romorgniz for a full refund.
A New Life Herbs recalled 49 bottles of Baby Soothe Herbal Supplement on November 20, 2025. The product misbrands due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using the product immediately and seek a refund.
Face Rock Creamery recalled 16 units of Vampire Slayer Garlic Cheddar Cheese, 6 oz, distributed in Oregon after an FDA environmental sample detected Listeria monocytogenes in the packaging area. The hazard is a contamination risk that could cause life-threatening infection in some populations. Consumers should not eat the cheese and should contact Face Rock Creamery for a refund or replacement.
Shantou Chenghai Xingzigu Toy Industry recalled Bettina Doll Sets sold on Amazon after finding the unicorn’s battery compartment is easily accessed by children. Button cell batteries can cause serious injuries or death if swallowed. Stop using the recalled toys and request a full refund by emailing bettinaaftersales@outlook.com.
Zippee silicone activity toys imported by Mobi Games are recalled due to a choking hazard. The recall involves a teal silicone cylinder with six string holes and spherical ends on five strings. Stop using the recalled toy immediately and contact Mobi Games for a full refund.
Zigjoy-US recalls Zigjoy-branded children's sleep sacks sold online after risk of serious burn injury. The recall covers blue sleep sacks with an excavator print and pink with a bunny print in sizes S, M, and L. The products claim 100% cotton on sewn-in labels. Consumers should stop using them immediately and seek a full refund.
Jeni's Splendid Ice Creams recalls Passion Fruit Dreamsicle Ice Cream Bars for undeclared wheat and soy allergens. The recall covers 3,767 cases distributed to 10 states. Consumers should not eat the product and should seek a refund or replacement via email.
Nissan North America recalls 2025 Kicks vehicles due to a Shift-to-Park warning that may not activate when the vehicle is shut off in a gear other than Park. The recall targets 2025 Nissan Kicks. Nissan will reconfigure the BCM to activate the warning at no cost. Notifications began January 29, 2025, with more letters expected May 7, 2025.
Toyota Motor Engineering & Manufacturing recalls multiple 2023-2025 vehicles because the instrument panel may fail to display speed, braking and tire pressure alerts. Dealers will update software for non-PHEV models and inspect/possibly replace panels for PHEV models at no charge. Owner letters expected Oct 27, 2025. Contact Toyota at 1-800-331-4331; Lexus follow numbers 25LB05/25LA05.
ByHeart announced a recall of over 6.9 million units of its infant formula on November 8, 2025, due to contamination with Clostridium botulinum. The recall affects both cans and single-serve packets sold nationwide. Parents are urged to stop using the affected products immediately to prevent serious health risks.
Pacific Seafood recalled 15,498 pounds of Raw Blackened Shrimp Peeled & Deveined Tail-Off sold refrigerated after undeclared sulfite was detected. The product is a shrimp tray produced in Ecuador and distributed in Alabama, Florida and Massachusetts. Consumers should not eat the product and should contact Pacific Seafood Group for a refund or replacement.
Costco Wholesale recalled 612 units of Kirkland Signature Chicken Sandwich with Caesar Salad distributed in New York and Puerto Rico. The 3-ounce Caesar Dressing packet in the sandwich may contain plastic material. Consumers who bought the product should not consume it and should contact Costco for a refund or replacement.
The recall involves Neaude BR0221SL001 adult portable bed rails sold on Amazon. It poses a serious entrapment and asphyxiation risk. Consumers should stop using the recalled rails and start the refund process with Neaude now.
Fresenius Kabi USA, LLC recalls 2,199,850 vials of Famotidine Injection, U.S. distribution nationwide plus Alaska, Hawaii and Puerto Rico after endotoxin testing concerns. The microbial contamination risk prompted an immediate stop-use order. Healthcare providers and patients should follow recall guidance and seek alternatives through their providers.