153 recalls tagged with “holiday product”.
JC Sales has issued an active recall for Lil' Buddies Pet Laser Toys, model 24496, sold by discount retailers nationwide. The recall cites serious injury or death risk from battery ingestion. The toys include three button cell batteries and fail to meet mandatory standards for teething toys.
Generac Power Systems recalls portable generators with orange/black covers due to risk of fuel leak during fueling. The recall covers specific unit types and model numbers within limited serial ranges. Stop using the recalled generators and check eligibility at Generac’s recall site for a free repair.
Seasonal Specialties recalled the Member's Mark 7-foot Pre-Lit Twinkling Buck sold online at Sam's Club after a burn hazard was identified. The recall centers on wiring that can overheat if connected incorrectly. Consumers should stop using the Buck immediately and contact Seasonal Specialties for a full refund or a repair kit.
Silks recalled all children's two-piece loungewear sets sold online at Silksdesign.com. These sets violate mandatory flammability standards for children's sleepwear and pose a serious burn risk. Parents should stop using the recalled loungewear immediately and contact Silks for a full refund or store credit.
Wybotics is recalling specific Osprey 700 Max and S1 robotic pool vacuums sold through retailers after reports that the lithium-ion battery can overheat, creating a burn and fire hazard. The recall covers Osprey 700 Max models WY3312MAX and WY100MAX and S1 WY200, with serial numbers WY100M230117XXXX, WY100M230127XXXX, WY100M230130XXXX, WY100M230318XXXX, WY200-230328XXXX and W200**230330XXXX. The U
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.
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.
House of Flavors recalled 4,880 tubs of Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub, distributed in Illinois. The product contains undeclared egg. Consumers should not consume it and should contact House of Flavors for refund or replacement via email.
HEYTEA USA INC recalls 12,677 cartons of Coconut Drink 1 sold for catering establishments in multiple states after undeclared milk was found. The product contains milk not listed on the label. Consumers should not consume the product and contact HEYTEA USA INC for refund or replacement by email.
Sunnyyes LED mini lights are recalled after reports of serious injury risk from accessible coin batteries. The recall covers Sunnyyes branded lights sold nationwide. The hazard stems from lithium coin batteries accessible to children, plus a loose remote-control battery screw and missing parental warnings. Stop using the product and contact Sunnyyes for a full refund.
Electrolux Group recalled Frigidaire gas ranges sold nationwide through retailers after a burn hazard was identified. The bake burner can ignite with delay, creating a burn risk. Stop using the recalled ovens immediately and contact Electrolux for a free in-home bake burner repair; cooktops remain usable.
Pocas International Corp. recalls 148 cases of POPPING BOBA RTD Mixed Berry Hibiscus Tea distributed to New York, Virginia, Florida, Massachusetts, Texas, Louisiana, Utah, California and Canada. A packaging integrity issue may compromise product quality. Consumers who purchased should not consume it and should contact Pocas International for refund or replacement information via email.
FDA analysis found undeclared sildenafil and tadalafil in Boner Bears Honey 100% Wildflower Honey. The recall covers 15-pouch boxes manufactured in Florida with distribution in New Jersey. Consumers should stop using the product and seek refund or replacement from Pure Vitamins and Natural Supplements.
Cook Medical recalled 49 units of the Strange Bile Duct Stone Exploration Set due to labels showing expiration dates beyond shelf life. The recall is worldwide and active as of March 5, 2026. Healthcare providers were advised to stop use and follow recall instructions.
KC Pharmaceuticals recalled 182,424 Sterile Eye Drops AC bottles sold nationwide under multiple brands including Quality Choice Eye Drops Irritation Relief and Goodsense Ultra Lubricant Eye Drops. The recall cites a lack of assurance of sterility. Consumers should stop using the product immediately and contact KC Pharmaceuticals for guidance.
Ajinomoto Foods North America recalls 3,059,808 pounds of Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed sold nationwide after glass fragments were found in the product. The glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the product and should seek a refund or replacement. The recall number is H-0591-2026.
Philips recalls 298 Azurion 3 M12 X-ray imaging systems used by healthcare providers worldwide. The issue is that X-ray imaging may not start or may be intermittent when using the wired foot switch. Stop using the affected devices immediately and follow recall instructions from Philips.
Goodsense Eye Drops Original Formula, distributed nationwide, has recalled 378,144 sterile bottles in 2026 due to lack of assurance of sterility. The sterile ophthalmic solution may be contaminated. Consumers and healthcare providers should stop using immediately and contact K.C. Pharmaceuticals for refunds or replacements.
Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold in the United States and internationally after determining the Obstruction Alarm may fail to trigger within required standards. The alarm can delay alerting caregivers for up to four breaths. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Philips or their clinician.
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,