153 recalls tagged with “holiday product”.
Tegu recalled two Magnetic Floating Stackers sold at multiple retailers. Models STA-BGY-801T and STA-BTP-806T are affected. The magnets can detach and be ingested, posing a serious injury or death risk. Parents should stop using the toys immediately and contact Tegu for a free replacement.
Baby Loren recalls four Morning children’s 100% cotton loungewear dresses in 2025 for fire safety violations. The recall involves dresses with neck labels listing October 2022 or October 2023 and batch numbers ending in 3465, 3585, 3599 or 3569. Consumers should stop using the dresses and contact Baby Loren for a full refund.
Dynamic Sports Nutrition recalled 1,566 bottles of WINN-50 vanazolol dietary supplement sold nationwide. The FDA-listed recall cites degradation of an ingredient and sub-potent Vitamin B12. Consumers should stop using the product and contact the company for refunds or replacements.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes for external use. The U.S. FDA listing cites lack of assurance of sterility as the reason for recall. Consumers and healthcare providers should stop using this product immediately and contact the manufacturer for guidance.
Bestway, Intex and Polygroup recall 5 million above-ground pools taller than 48 inches after nine deaths. The recall covers pools whose model numbers are printed on the liner outside the pool. The hazard stems from a compression strap around the pool legs that can create a foothold for a child, enabling access to the water. Stop using the pools immediately and contact the respective brands for a维修
Quest International recalls 376 Measles IgM ELISA kits nationwide in Utah, Texas and Arizona after discovering the product lacks premarket approval or clearance. The high-risk health device carries a Class II designation. Stop using the device immediately and follow manufacturer recall instructions.
BioFire Defense recalled 130 FilmArray NGDS Warrior Panel NGDS-ASY-0007 kits distributed nationwide in the United States. The recall cites an increased risk of internal control failures when testing positive blood cultures. Clinicians should stop using the device immediately and follow recall instructions provided by BioFire Defense. Notification is by letter to affected facilities.
Boothwyn Pharmacy recalls 8 vials of Fluorescein 2% Ophth 3 mL nationwide after a subpotent drug finding. The recall was issued July 9, 2025 and remains active.
Walmart’s ReliOn sterile alcohol swabs are recalled nationwide due to subpotent isopropyl alcohol. The FDA notice lists 3,456,000 pads affected across 4,800 per case and 24 boxes per case. Consumers should stop use and contact Medline Industries or a healthcare provider for guidance.
Chefs Warehouse recalls 15 pounds of cucumber slices after Salmonella contamination was detected. The recall covers 10-pound and 5-pound packages labeled 5# Lot#B0515465 and 5# Lot#B0515867 distributed to Maryland, Delaware and Virginia. Consumers should not consume the recalled cucumbers and should contact Chefs Warehouse for refund or replacement.
Chefs Warehouse recalled 15 lbs of diced cucumbers distributed to Maryland, Delaware and Virginia after Salmonella contamination was found. The recall is active as of May 20, 2025. Consumers should not consume the product and should contact Chefs Warehouse for refund or replacement.
Turkana Food Inc. recalled 352 cases of Floria Dried Apricots, 200-gram packages, distributed to retailers in 19 states. The recall was issued on April 29, 2025. The product contains undeclared sulfites. Consumers should not eat it and should contact Turkana Food Inc. for refund or replacement via email.
MEDITECH released an active recall for the Expanse Laboratory calculator/data processing module. The recall covers 148 units distributed worldwide, including the US, UK, Canada, Ireland and the British Virgin Islands. The hazard concerns simultaneous multi-key inputs potentially removing data from the first field in screens or questionnaires.