794 recalls tagged with “infant product”.
Nexgrill recalls more than 10.2 million metal wire bristle grill brushes sold at Home Depot. Bristles can detach and stick to food or grills. Consumers should stop using recalled brushes and contact Nexgrill for a full refund issued as a gift card.
Petzl America recalls Nomic and Ergonomic ice climbing axes due to a shaft break risk that could cause a fatal fall. The recall involves specific serial ranges across two models and targets accessories sold through specialty retailers and online shops. Consumers should stop using the axes and pursue a free repair kit from Petzl America.
Sunnyyes LED mini lights are recalled after reports of serious injury risk from accessible coin batteries. The recall covers Sunnyyes branded lights sold nationwide. The hazard stems from lithium coin batteries accessible to children, plus a loose remote-control battery screw and missing parental warnings. Stop using the product and contact Sunnyyes for a full refund.
Vive Health recalled adult portable bed rails after two deaths were linked to entrapment and asphyxiation. The recall covers the Compact Bed Rail model LVA2009SLV, Bed Rail Collection V model LVA2097SLV, and LVA1024 units purchased on or before August 21, 2023. A prior recall covered LVA1024 units purchased after that date. Consumers must stop using these rails and seek a full refund from Vive.
Connecticut Crab Company LLC recalls 39 boxes of crab cakes sold to food service due to potential temperature abuse that could enable Clostridium botulinum growth. The recall notice is active as of April 15, 2026. Consumers who purchased these products should not consume them and should seek refund or replacement information from the company.
GE Healthcare recalled Omnipaque iohexol injection, 300 mg/mL, distributed nationwide in the United States. The Class II recall covers 866,570 vials due to particulate matter. Healthcare providers should stop use and contact GE Healthcare Ireland Limited for guidance.
GE Healthcare recalled Omnipaque iohexol injection after discovery of particulate matter. The recall covers 306,810 vials distributed nationwide in the United States. WHS: Distributed by GE Healthcare Inc., Marlborough, MA. Consumers should stop use and consult a healthcare provider for guidance.
Fagron Compounding Services recalled 34,260 bags of Vancomycin HCI Injection across the United States. The recall cites lack of sterility assurance and a blue Break-Off-Part that could detach from the administration port. Healthcare providers and patients should stop using the product immediately and follow manufacturer guidance.
Fagron Compounding Services is recalling 11,680 bags of Vancomycin HCl 1 g in 250 mL 0.9% Sodium Chloride Injection. The recall is nationwide in the United States. The blue break-off part could detach from the administration port, raising sterility concerns. Stop using immediately and contact the provider for guidance.
Fagron Compounding Services recalled 5,140 bags of norepinephrine Bitartrate injection due to lack of sterility assurance. A blue Break-Off-Part could detach from the administration port. The recall covers nationwide distribution in the U.S. Consumers should stop use and contact providers for guidance.
Teva-affiliated Clonidine Transdermal System recalls 113,943 cartons after CGMP deviations. Unapproved raw material prompts recall. Stop use immediately and contact Teva or a healthcare provider for guidance.
Wagner Spray Tech recalls 900 Series power steamers, including the 905e Auto Steamer, 915e On-Demand Power Steamer, and 925e Steam Machine Elite Steamer. The recall cites a burn hazard from an overheating hose and hot-water expulsion from the nozzle. Consumers should stop using the recalled steamers immediately and contact Wagner for a free repair kit.
Goregent is recalling Goregent-branded infant walkers sold on Amazon. The recalled walkers can fit through a standard doorway and fail to stop at the edge of a step. Parents should stop using the recalled walkers immediately and contact Goregent Official Store for a full refund.
Electrolux Group recalled Frigidaire gas ranges sold nationwide through retailers after a burn hazard was identified. The bake burner can ignite with delay, creating a burn risk. Stop using the recalled ovens immediately and contact Electrolux for a free in-home bake burner repair; cooktops remain usable.
Tainoki Fine Furniture recalled three office chairs sold at HomeGoods stores nationwide from August 2025 through December 2025 for about $180 to $200. The base can bend, creating a fall hazard. Stop using the chairs immediately and follow the recall instructions on the company site for a full refund.
Lifetime Brands recalls BUILT LUUM Light Up Tumblers sold at multiple retailers. The recall covers 16 oz and 18 oz plastic cups with a lid and straw that contain a bottom LED light powered by a button cell battery. Labels on the underside or hangtags show the theme and item numbers with UPCs. Stop using these tumblers immediately and seek a full refund by contacting Lifetime Brands.
Teva Pharmaceuticals recalled 21,930 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the United States. The recall stems from lack of assurance of sterility identified during an FDA inspection at the contract manufacturer. Healthcare providers and patients should stop using this product immediately and contact Teva or a physician for guidance.
Chiesi USA recalled 7,235 Curosurf vials distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Chiesi USA for guidance.
Teva Pharmaceuticals USA recalled 19,869 cartons of Octreotide Acetate for Injectable Suspension nationwide in the United States after FDA inspection flagged lack of assurance of sterility at the contract manufacturer. The FDA cited quality system deficiencies at Pharmathen International S.A. in Greece. Healthcare providers and patients should stop using the product immediately and contact Teva or
Xanax XR extended-release alprazolam recall issued March 17, 2026 remains active. Viatris Specialty LLC distributes the drug nationwide in the United States. The issue is failed dissolution specifications. Patients and healthcare providers should stop using the product immediately and follow the recall instructions for guidance.