266 recalls tagged with “children product”.
DT Swiss recalled carbon road wheels sold aftermarket and on high-end bikes due to a wheel integrity defect that can cause a crash. The recall covers wheels with DT Swiss ID codes of 2740000 or higher. DT Swiss provided a replacement remedy. Consumers should stop riding recalled wheels and contact DT Swiss for a replacement.
Siemens Medical Solutions USA recalled 9 MAGNETOM Cima.X MRI systems worldwide. A potential ice blockage in the magnet venting system could prevent helium from escaping during a quench, risking rupture and a helium leak into the scanning room. Hospitals and healthcare providers should stop using the devices and follow the manufacturer’s recall instructions.
Siemens Medical Solutions USA recalls 69 MAGNETOM Verio MRIs worldwide after an ice blockage could trap helium gas during a quench. A rupture of the helium containment system may leak helium into the scanning room. The recall affects models with number 10276755 and serials including 40649 and others. Patients and providers should stop using the device and follow manufacturer instructions.
Boston Scientific recalled 28,911 pacemakers worldwide due to a software flaw in Safety Architecture that could prevent Safety Mode when battery impedance is high. The recall covers ACCOLADE family devices and VISIONIST and VALITUDE CRT-Ps. Patients should stop using the device immediately and follow the recall letter instructions.
Aesculap AG recalls the ELAN 4 Fixed Duraguard Long device, Model GB943R, after mislabeling errors were discovered. The U.S. distribution reached Missouri with international distribution to multiple countries. Healthcare providers should stop using the device immediately per manufacturer instructions.
STWUQIKONG recalled a three-tier spiral tower toy sold on Shein because of a choking hazard. The recall was announced on August 14, 2025. The toy includes three yellow balls and is designed for children under three, violating the small-ball ban. Stop using the product immediately and email STWUQIKONG_RECALL@hotmail.com to receive a full refund.
Firefly Fuel Inc. recalled Firefly Safe & Green 32 oz. bottles. The recall date is August 14, 2025. The fuel is sold in a clear bottle with a white cap and nozzle applicator. The product label shows Firefly brand, Safe & Green in green font, and claims Non-Toxic and Kosher. The nozzle applicator lacks child-resistant features, violating the Poison Prevention Packaging Act and the Federal Hazardous
Novartis Manufacturing NV and Sandoz Inc recall ciprofloxacin 0.3% and dexamethasone 0.1% otic suspension after temperature abuse. The recall affects one consignee in California. Consumers and health care providers should stop using the product immediately and follow guidance from Sandoz or a healthcare provider.
Philips North America has issued a recall for 81 IQon Spectral CT systems, Model 728332, sold worldwide. The patient support table may descend unexpectedly to the lowest position due to ball screw misalignment after a replacement. Stop using the device immediately and follow manufacturer recall instructions.
Applied Medical Technology recalled 840 NutraGlide ENFit nasal feeding tubes distributed in the United States to Massachusetts and Rhode Island. The tubes have distal tips that may detach at lower than expected forces. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.
Applied Medical Technology recalled 200 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. The distal tips may detach at lower than expected forces. Stop using the device immediately and follow the manufacturer’s recall instructions.
Applied Medical Technology recalled 1,780 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. Distal tips on these devices may detach at lower than expected forces. Stop using immediately and follow the recall instructions.
Séfralls Minoxidil Hair Generation Serum, sold by Guangzhou Ariel Biotech, was recalled on August 7, 2025. The serum is packaged in amber dropper bottles with a white and gold dropper and a white, black and gold label. The packaging is not child-resistant, violating the Poison Prevention Packaging Act and creating a poisoning risk for children. Consumers should stop using the serum immediately and
TEMI Toys recalled the TEMI Go Basketball toy sold on Amazon due to a choking hazard for children under three. The toy stands about 13 inches tall and 4 inches wide and includes three yellow balls. TEMI Toys is offering a full refund to consumers who stop using the product and contact the company.
Monica Vinader recalls select 14k yellow gold mini heart bracelets, necklaces and stud earrings due to high cadmium levels. The recalled jewelry was manufactured in October and November 2024. Consumers should stop wearing the jewelry immediately and contact Monica Vinader for a replacement or refund.
La Ligne recalls Enfant Bonne Nuit children’s pajamas after a burn hazard was identified. The recall covers La Ligne by La Ligne Enfant Bonne Nuit two-piece sets sold in various colors. Consumers should stop using the pajamas and pursue a full refund or store credit.
Deale International recalls Altafit AF28 smartwatches sold by HSN after reports of overheating charging pads. The recall cites a risk of serious burn injury and fire. Consumers should stop charging the watch immediately and contact Deale International for a free replacement.
AliExpress recalls LeymanKids children's two-piece pajama sets sold online. The recall stems from a violation of mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and pursue a full refund through AliExpress.
SeaSpine Orthopedics recalled 74 Reef TA Inserter instruments used with the Reef Interbody System, distributed worldwide to hospitals and surgical centers. The inserter may cause difficulty disengaging the implant or improper positioning, prolonging surgery and possibly requiring intraoperative revision. Hospitals and surgeons should stop using the device and follow recall instructions from SeaSpn
Boston Scientific recalls 39,739 Encore 26 Inflation Devices worldwide after an internal investigation found foreign material particles could migrate from the device into balloon dilation catheters. The high-severity recall affects interventional cardiology and peripheral interventions devices. Stop using immediately and await recall instructions from Boston Scientific or healthcare providers.