Every parent needs to see this: 353 high-risk children's product recalls currently active. Check your home now.
386 baby and children's product recalls tracked. Protect your kids from dangerous toys, cribs, car seats, furniture, and other hazardous products.
Every year, emergency rooms treat approximately 150,000 children under age 15 for toy-related injuries, according to the Consumer Product Safety Commission (CPSC). Many of these injuries could be prevented with better awareness of product recalls and safety standards.
Children are uniquely vulnerable to product hazards because they explore the world by touching, tasting, and testing everything around them. Products designed for adults may pose unexpected risks when children gain access to them, and even products specifically made for children can have manufacturing defects or design flaws.
Staying informed about recalls is one of the most effective ways to protect your children. When a recall is announced, the manufacturer has determined (or a government agency has found) that the product poses a genuine safety risk that warrants action.
Help other parents: Share this page with parent groups, playdate friends, and family members. Every parent deserves to know about these safety alerts.
Zarlengo Italian Ice recalled 757 units of chocolate gelato across multiple sizes in Illinois, Indiana and Texas. The issue centers on a soy lecithin omission in the contains statement. Consumers should not eat the product and should seek a refund or replacement.
Fourour Kiddies recalled tip restraint kits after tests found plastic components could break, creating a tip-over risk. The recall affects kits used to secure furniture to walls. Consumers should stop using the recalled restraints and seek a stainless steel replacement from 4our Kiddies.
AirClub recalled convertible bassinets that convert into bedside sleepers due to a hazardous attachment mechanism. The recall affects models labeled QX-831. The defect creates an opening between the bedside sleeper and mattress, posing a risk of serious injury or death to infants. Stop using the product immediately and contact AirClub for a replacement attachment mechanism.
FUNTOK 24V 2-Seater Ride-On Trucks recalled by Shenzhen Luobe Trading Co. for fire and burn hazards. The recall covers model DLS-K03 sold in red, black, white and pink. The company urges consumers to stop using the product and contact for a full refund.
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.
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.
Riverence Provisions LLC recalls 3,672 units of Smoked Trout Dip sold frozen in cases distributed to eight states over milk allergen labeling. The recall is active as of April 15, 2026. Do not consume the product. Contact Riverence Provisions for refund or replacement.
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.
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.
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 recalled 1,897 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the USA after an FDA inspection flagged sterility concerns. The recall is due to lack of assurance of sterility from the contract manufacturer. Consumers and healthcare providers should stop using the product immediately and contact Teva for guidance.
Cipla USA Inc. recalls 54,583 Lanreotide acetate injections nationwide after FDA flagged sterility assurance concerns at a contract manufacturer. The recall covers a box containing one pre-filled syringe and one safety needle. Healthcare providers and patients should stop using the product immediately and follow the company’s guidance for disposal and refunds.
Stryker Sustainability Solutions recalled 56,740 color cuff tourniquet cuffs due to potential detachment from the bladder. The recall affects 18" and 24" cuffs across multiple U.S. states. Patients and healthcare providers should stop using these devices immediately and follow manufacturer instructions.
17 Stories Furniture recalled its 14-drawer dressers on March 12, 2026, due to serious tip-over hazards. The dressers, sold in black, white, and brown, can pose risks of injury or death to children if not anchored. Model numbers include 55SCDR14KDBRDL and 55SCDR14KDCHDL.
LIVEHOM recalled 11-Drawer Dressers on March 12, 2026, due to tip-over hazards. The recall affects dressers sold on Amazon that can pose serious risks to children. Consumers must stop using these dressers immediately and contact the company for a full refund.
LFTE USA recalled Playground Swing Set Seats on March 12, 2026. The swing seats pose a fall hazard due to potential rivet failure. The recall affects model number 999604 with the code 'LF-65708' marked on the seat pad.
ProRider recalled several models of bicycle helmets on March 12, 2026, due to a serious risk of head injury. The helmets do not meet mandatory safety standards and can fail in a crash. Consumers should stop using these helmets immediately and seek a refund.
Stoney Games recalled Kluster Fun Tabletop Magnet Chess Games on March 12, 2026, due to a serious ingestion hazard. The games contain loose, high-powered magnets that can be swallowed by children, posing a risk of severe injury or death. Consumers should immediately stop using the games and contact Stoney Games for replacement options.
Fresenius Kabi USA recalled 0.9% Sodium Chloride Injection nationwide, including Alaska and Puerto Rico. The recall is due to lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Fresenius Kabi for guidance.
Fresenius Kabi USA recalls 0.9% Sodium Chloride Injection units distributed nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers should stop use and contact Fresenius Kabi for guidance.
Cook Medical recalled 5,080 Spectrum Central Venous Catheter Sets worldwide after labeling that indicated expiration dates beyond the products' true shelf life. The recall alerts patients and healthcare providers to stop using affected lots and follow manufacturer instructions.
Cook Medical recalled 916 units of the Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set worldwide after discovering expiration dates exceeded true shelf life. The recall affects multiple reference part numbers and order numbers. Healthcare providers should stop using the device immediately and follow Cook’s instructions for recall notification.
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