33 recalls tagged with “toddler product”.
Shenzhen Baihang recalled VEEKTOMX VT103 Mini Power Banks sold on Amazon. The recalled devices contain a lithium-ion battery that can overheat and ignite. Consumers should stop using the recalled power banks immediately and contact Shenzhen Baihang or Veektomx for a free replacement.
Sam's Club recalls Member's Mark Valentine pajama sets due to burn risk and a violation of mandatory flammability standards for children's sleepwear. The recall covers sizes XS through XL sold online between December 2025 and January 2026 for about $14. Consumers should stop using the pajamas immediately and contact Sam's Club for a full refund.
Coluans recalled Christmas Light-Up Rings sold on Amazon by BUDI Official. The recall centers on a battery ingestion hazard from three preinstalled button cell batteries visible through the ring’s clear casing. Stop using the rings immediately and return them for a full refund by emailing BUDIrecall@outlook.com with a photo of the disposed product.
TecFlox recalled its Minoxidil Topical Solution hair growth serum bottles on April 2, 2026. The packaging is not child-resistant, violating the Poison Prevention Packaging Act. Consumers should stop using the product immediately, store it out of reach of children, and email TecFloxrecall@outlook.com to receive free replacement bottles. Only bottles with serum remaining will be replaced; dispose of
Gavoyeat recalled 50-ring Halloween Light-Up Rings sold on Amazon by CSZWEICD on April 2, 2026. The recall cites a battery ingestion hazard from an accessible button cell battery in the ring’s housing. Stop using the recalled rings and return them for a full refund by emailing recalledgavoyeat@yeah.net.
General Motors recalled certain 2024 Chevrolet Silverado EV and 2024-2025 GMC Sierra EV pickup trucks due to a seat belt safety issue. The recall affects vehicles still in dealer inventory, with no owner letters mailed. Owners can contact GM customer service for further assistance.
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 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.
Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.
Philips Medical Systems Nederland recalled 5,167 Azurion 7 M20 X-ray imaging systems sold to healthcare facilities in the U.S. and internationally. The wired foot switch can fail to initiate imaging or produce intermittent imaging. Hospitals and clinics should stop using the device and follow recall instructions from Philips, with notification by letter to affected parties.
American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,
Olympus recalls 7 PKS Cutting Forceps worldwide because welded components may fail. The devices are used with a 5mm cannula and an electrosurgical generator. Stop using the device and follow the manufacturer’s recall instructions. Healthcare facilities should verify device details and consult Olympus for replacement options.
Yiruikeji2024 recalled magnetic chess games on February 24, 2026, due to ingestion hazards. The games contain loose magnets that can pose serious health risks to children. Consumers should stop using the product and seek a refund immediately.
Medline Industries is recalling 14,379 kits nationwide that include Olympus biopsy valves. The recall follows reports of rubber fragments detaching from the valves during use. Healthcare providers and patients should stop using the affected kits and follow Medline’s recall instructions.
Medline Industries recalled 651,789 ENFIT G-TUBE connectors (ENFIT1010GC) sold worldwide, including the United States and Canada. The connectors were not manufactured to required dimensional specifications and may not seal properly with ENFit-style devices, which could lead to leakage. Healthcare facilities and patients should stop using this device immediately and follow recall instructions from
Erbe USA recalled 2,408 Flexible Cryoprobes (REF 20402-411) used in surgery nationwide, including Puerto Rico. Probes may rupture or burst during activation. Hospitals and healthcare providers should stop using the device and follow recall instructions. Manufacturer contact will provide remediation.
Reflexion Medical recalled 12 RefleXion X1 Radiotherapy System RXM1000 units sold to hospitals and healthcare providers in the United States after a software defect could cause a 5mm or greater misalignment and underdose. The defect occurs during angular roll corrections followed by a repeat localization, and the roll corrections from the initial localization are not carried through to treatment.
Olympus Corporation of the Americas recalls 1,276 boxes of MAJ-1218 Single Use Biopsy Valve distributed nationwide to healthcare facilities. The device risks rubber fragment detachment during use. Stop using the device and follow the recall instructions from Olympus or your healthcare provider.
Mangalm LLC recalled Tops GOLD Mixed Pickle sold in California, Nevada, Oregon, Utah and Washington after FDA enforcement. The product may be adulterated with erucic acid from mustard oil. Consumers who purchased it should not eat it and should contact Mangalm for refund or replacement via email.
I.T.S. recalled 46,637 pelvic reconstruction system components nationwide in the United States after MRI safety testing showed higher RF-induced heating than the IFU stated. The issue centers on MRI heating under certain conditions that could injure patients. Patients should stop using the devices and follow manufacturer recall instructions.