224 recalls tagged with “pet related”.
Baker’s Authority recalled 70 units of Graham Cracker Meal on August 12, 2025. The product ships to multiple states. Undeclared wheat and soy allergens are listed on the label. The recall urges consumers to avoid consumption and seek refunds or replacements.
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.
Petmate recalled Pet Zone Laser Pointer & LED Ball toys sold exclusively at Menards. The recall date is August 7, 2025. The products contain six preinstalled button cell batteries and pose an ingestion hazard if the battery compartment is breached. Consumers should stop using the recalled toys and contact Petmate for a full refund.
Westminster Pharmaceuticals recalls 16,672 boxes of Metoprolol Tartrate 50 mg tablets nationwide after nitrosamine exceeds Acceptable Daily Intake. Manufactured by Renata PLC in Bangladesh and distributed in the US by Westminster Pharmaceuticals. Consumers should stop using the product and contact their healthcare provider for guidance.
Hi-Tech Pharmaceuticals recalled 85,950 units of Pine Bark Supplements for unapproved drug claims and misbranding. The FDA enforcement notice lists Hi-Tech Pharmaceuticals, Inc. of Norcross, GA as the marketer. The recall cites unapproved drug claims and misbranding as the reason. Consumers should stop using the product and contact the company for refund or replacement information.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Quercetin dietary supplement distributed to 40+ states after FDA enforcement found unapproved drug claims and misbranding. The recall, active as of Aug 6, 2025, stems from regulatory concerns rather than a reported health incident. Consumers should stop using the product and contact the company for refunds or replacements.
Boston Scientific recalled 1,369 Encore 26 Inflation Devices used with balloon dilation catheters after an internal investigation found foreign material particles could migrate into a balloon dilatation catheter. The recall affects 12 UPNs including M0062251200 through M0062251370. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.
Amazon recalled Amazon Basics Premium Foam Eurotop Mattresses sold on Amazon. The nine-inch mattresses in twin, full, queen and king sizes were manufactured from 12/22/2022 through 05/16/2024 and violate the federal flammability standard, posing a fire hazard. Stop using the recalled mattress and contact Amazon for a full refund.
Pfizer's Levoxyl 50 mcg levothyroxine tablets are recalled due to subpotency. About 29,004 bottles distributed in the U.S. since distribution. Consumers should stop use and contact their healthcare provider for guidance.
VITROS Chemistry Products LAC Slides recalled after calibration failures on VITROS XT 3400 and VITROS XT 7600 systems. The recall covers catalog 8433880 with 2,908 units distributed nationwide in the US. Manufacturers warn that coating 0130 and above with Condition Code TH4-63J elevates calibration failures, delaying lac test results and potentially impacting patient management. Health providers,病
BMW recalls 2025 motorcycles with optional eCall system due to a software error that can deactivate emergency crash notification. OTA or dealer update will fix the issue. Letters to owners go out Sept. 12, 2025. Contact BMW at 1-800-525-7417.
Home Health US recalled 4,661 One Step Sterile Lancets for Single Use sold nationwide through Amazon. The recall cites incorrect or missing Unique Device Identifier codes. Consumers should stop using the lancets immediately and follow the recall instructions from Home Health US or their healthcare provider.
Summa Therapeutics recalled 22 units of the Finesse BTK Multicath Injectable Angioplasty Balloon Catheter sold to healthcare facilities in New Jersey and Florida. The balloon may not meet burst specifications, raising risk during angioplasty. Healthcare providers must stop using the device immediately and follow recall instructions from Summa Therapeutics.
DermaRite Industries recalled 249 bottles of DermaSarra External Analgesic on July 17, 2025 due to microbial contamination. The product, sold nationwide, carries NDC 61924-189-08 and Lot 40187.2 with an expiration date of February 2026. Consumers should stop using the product immediately and contact DermaRite for guidance.
Creekliybear recalled its Pack and Play aftermarket mattresses sold on Amazon by Kbabyea on July 10, 2025. The mattresses exceed thickness standards and may not fit certain play yards, creating a suffocation entrapment risk. Parents should stop using the mattresses immediately and contact Kbabyea for a full refund.
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.
Tandem Diabetes Care recalls 19 units of the t:slim X2 insulin pump with interoperable technology distributed internationally, including Israel. An app defect occurs when the phone uses a right-to-left language and can cause app-pump pairing problems and graphical defects. Patients should stop using the device immediately and follow the manufacturer’s recall instructions.
CHETAK NEW YORK LLC recalled 5,232 packets of Deep Sprouted Mat 16 oz distributed to California, New Jersey, Illinois, Florida and Texas after tests found Salmonella. The recall class is I with a high hazard level. Consumers should not consume the product and should seek refund or replacement by email.
Vitalabs recalled 9,657 bottles of Vitamin B12 Raspberry Gummies sold under Black Girl Vitamins and Rise-N-Shine brands after suppliers flagged undeclared peanuts. The product may contain peanuts not disclosed on the label, creating a peanut allergy risk. Consumers should stop using the product and contact Vitalabs for refund or replacement.
Sedecal SA recalled 1 mobile X-ray system in the United States. The device is distributed in CA, IL and NJ. The system is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could have unspecified consequences. Clinicians and facilities should stop using the device and follow manufacturer instructions.