Pet food recalls
25 recalls.
- Wechem Hand Guard8/1000mL Bag recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Spurrier recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Lynx recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Lynx recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Lynx recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Certus Medical Satin Foam recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Aero Foamy Mango Aloe Vera Antiseptic Hand & Body Wash recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Aerocare Sani Mango Antiseptic Hand and Body Wash recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - Palm Antiseptic Hand Soap Net Contents: 1 Gallon recall (ABC Compounding Co., Inc.)
DrugClass IIReported November 4, 2026 · CGMP Deviations - SOUP MIX-6/58oz Tray recall (NatureBest Pre-Cut & Produce LLc)
FoodClass IReported September 23, 2026 · Jalapenos have the potential to be contaminated with Salmonella - Zen Principle Naturals Moringa Leaf Powder dietary supplement recall (FACTORY6, INC.)
FoodClass IReported August 12, 2026 · Possible Salmonella in Moringa Leaf Powder product. - Vitamin B-Complex recall (Llorens Pharmaceuticals International Division, Inc.)
FoodClass IIReported May 27, 2026 · Foreign object: black particulate matter - ABC Trading Recalls Children's Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
Consumer productReported May 26, 2026 · The recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries... - Medline Kits: 1) MTS LEFT HEART KIT-CAROLINAS HOS recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - JC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported April 17, 2026 · The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate... - Sanlebi Pet Vet Playsets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Letokids
Consumer productReported April 17, 2026 · The Pet Vet Playset violates the mandatory standard for toys because the button cell batteries in the nail grinder and otoscope can be easily accessed by... - Valley Springs 100% Natural Bottled Water packaged in the following size plastic jug... recall (Valley Springs Artesian Gold, LLC)
FoodClass IIReported March 4, 2026 · Water was bottled under insanitary conditions. - Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number: 81559 ... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog Number:... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges ... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 ... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number: 81557 ... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model/Catalog... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number:... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - GE Healthcare Omni Legend recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 28, 2026 · There is a potential intermittent issue on certain Omni Legend systems that can result in a streaking artifact in the PET clinical scan images. This streaking...