Zarlengo Italian Ice Gelato Recalled in IL, IN, TX Over Soy Lecithin Disclosure Error (2026)
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Every parent needs to see this: 351 high-risk children's product recalls currently active. Check your home now.
384 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.
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.



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.


Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Label declares cream cheese but does not declare milk



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.
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.


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.

Lack of Assurance of Sterility
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.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
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