224 recalls tagged with “pet related”.
ZOLIQUEX recalled adult portable bed rails sold on Amazon after reports of entrapment and asphyxiation risk. The recall targets silver bed rails measuring 12.4 inches wide by 33.07 inches tall and weighing 7.1 pounds. The model numbers ZEX014-V1 and the Zoliquex branding appear on packaging. Stop using the product and seek a full refund by contacting ZOLIQUEX.
ATOYUS recalled its wooden activity cubes after authorities identified a choking hazard from spherical mallet ends and detached xylophone screws and clock hands. The recall covers products sold on Amazon by Melofaver US. Consumers should stop using the toy immediately and return it for a full refund.
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.
Yeeluzan recalled two-pack pool drain covers sold on Amazon. The covers measure 8.7 inches in diameter and weigh 1.7 pounds. They are white ABS plastic and packaged as two-packs. Pool owners should stop using these recalled covers and request a full refund.
BMW recalls 2022-2025 IX, 2023-2024 I7, and 2022-2023 i4 electric vehicles sold at BMW dealerships. A high-voltage battery cell module may have been improperly assembled. This can stress the module frame and lead to module failure. Owners should contact BMW for a free replacement of affected modules; recall letters were mailed September 11, 2025.
Mercedes-Benz USA is recalling 2023-2025 EQS and EQE models, including the EQS SUV 580 4MATIC, to fix a battery-management software defect. The software may cause the high-voltage battery to shut down, potentially resulting in a loss of drive power. Owner notification letters were mailed July 5, 2024. Dealers will update the battery management system software free of charge. Owners should contact
F&S Fresh Foods recalled 325 ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwiches distributed in Oregon after sesame was not declared on the label. The issue involves sesame as an undeclared allergen in a product labeled to contain egg, milk, soy, and wheat. Consumers should not eat the sandwich and should contact F&S Fresh Foods for refunds or replacements.
OCUN NA recalled Condor HMS Triple Carabiners sold online and through climbing retailers after the gate may fail to close automatically. The carabiner features an independent internal wire gate and a triple locking action. Stop using the recalled carabiner immediately and contact OCUN NA for a free replacement.
GM recalls 2025 Chevrolet Equinox EV AWD due to brake software that may not engage braking as expected. Dealers will update the brake system control module software at no charge. Owner letters mailed Feb. 13, 2025. GM contact: 1-800-222-1020. NHTSA recall number 25V012000.
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.
Blueroot Health recalled Aller-C dietary supplement bottles after discovering undeclared allergens. The recall covers Aller-C bottles in 100-count and 200-count sizes distributed across 35 states. Consumers should not consume the product and should seek refund or replacement.
Zarlengo Italian Ice recalled 757 units of chocolate gelato across multiple sizes in Illinois, Indiana and Texas. The issue centers on a soy lecithin omission in the contains statement. Consumers should not eat the product and should seek a refund or replacement.
Connecticut Crab Company LLC recalls 39 boxes of crab cakes sold to food service due to potential temperature abuse that could enable Clostridium botulinum growth. The recall notice is active as of April 15, 2026. Consumers who purchased these products should not consume them and should seek refund or replacement information from the company.
Teva Pharmaceuticals USA recalled 19,869 cartons of Octreotide Acetate for Injectable Suspension nationwide in the United States after FDA inspection flagged lack of assurance of sterility at the contract manufacturer. The FDA cited quality system deficiencies at Pharmathen International S.A. in Greece. Healthcare providers and patients should stop using the product immediately and contact Teva or
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.
Western Mixers Produce & Nuts recalled 384 cases of First Street Chilli Spanish Peanuts after a glass fragment was found inside sealed containers. The recall covers two consignees and 53 retail locations nationwide. Consumers should not eat the product and should email the company for refund or replacement.
Stryker Sustainability Solutions recalled 56,740 color cuff tourniquet cuffs due to potential detachment from the bladder. The recall affects 18" and 24" cuffs across multiple U.S. states. Patients and healthcare providers should stop using these devices immediately and follow manufacturer instructions.
Siemens Medical Solutions USA recalled 758 units in the U.S. and 2,077 outside the U.S. of ARTIS pheno and ARTIS Icono imaging systems after a dose-display anomaly could misrepresent high X-ray doses. The devices may still be within regulatory dose limits, but the displayed dose may appear significantly higher. Clinicians should stop using the devices and await manufacturer guidance.
Philips Medical Systems Nederland B.V. recalled 3,552 Vue Motion V12 devices worldwide, including the United States. The recall is due to a potential that mis-ordered frames during dynamic cine runs may display out of sequence. Stop using the device and follow the recall instructions provided by the manufacturer.