266 recalls tagged with “children product”.
Fixwal recalled its 7-Drawer Dressers on February 5, 2026. The dressers pose severe tip-over and entrapment hazards, particularly to children. Consumers should immediately stop using these furniture units and seek a refund.
Andy & Evan recalled children’s pajama sets due to a burn hazard. The recall covers sizes 2T through 6X sold online and at multiple retailers from February 2024 through June 2025 for $13 to $58. Consumers should stop using the pajamas and seek a full refund.
Shintenchi recalled 30,000 6-drawer dressers on February 5, 2026. The dressers pose a serious tip-over and entrapment risk to children if not anchored to the wall. Consumers should stop using the dressers immediately and seek a refund.
Dresbe LED Christmas Headbands are recalled in 2026 after a battery ingestion hazard was identified. The recall covers a two-pack set labeled HB-052. Stop using the headbands and contact Dresbe for a full refund.
LuxJet recalled Submersible LED Lights on January 29, 2026, due to ingestion risks from lithium batteries. The recall affects sets of 10 lights sold with multiple batteries. Consumers must stop using the lights and return them for a refund.
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
Gazelle USA recalled Urban Arrow FamilyNext Pro Cargo E-Bikes on January 29, 2026. The recall affects models with Fidlock buckles that may fail to latch securely. Consumers must stop using these e-bikes immediately and seek repairs.
Primark recalled The Nightmare Before Christmas Glow-in-the-Dark Coloring Set due to a poisoning hazard. The crayons contain high levels of strontium and aluminum, posing risks if ingested. The recall affects products sold from October 2024 through July 2025.
Potential for rubber fragment detachment during use.
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
