Pet food and pet product recalls
1056 federal recalls on file. Federal recalls for dog and cat food, treats, chews, supplements, and pet products. Sourced from the FDA and USDA and translated into plain English.
- 2025-02-26FDA-DeviceAugustine Temperature Management, LLCClass IIHot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode, 82 cm (32"), REF US501, to prevent or treat hypothermia
There is over-molding that stabilizes the connection between the cable and cable-entry on the mattress. It turns out that after about a year of use, the connector cable on the mattress can experience the same type of deflection that caused the intermittent connection with the cables connecting to the ESU.
- 2025-02-26FDA-DeviceAugustine Temperature Management, LLCClass IIAugustine Surgical Inc. HotDog Return Electrode accessory connector cables, Model A138 used in conjunction with Warming Blankets and Mattresses.
Users were experiencing the following error message (M-0B-125) stated Check Neutral Electrode Contact .
- 2025-02-26FDA-DeviceAugustine Temperature Management, LLCClass IIAugustine Surgical Inc. HotDog Return Electrode accessory connector cables, Model A136 used in conjunction with Warming Blankets and Mattresses.
Users were experiencing the following error message (M-0B-125) stated Check Neutral Electrode Contact .
- 2025-02-19FDA-DeviceCardinal Health 200, LLCClass IICardinal Health Presource Kits: 1) KIT,DIEP FLAP , Catalog Number:PB23DFCM3; 2) KIT,DIEP FLAP , Catalog Number:PB23DFCM4; 3) KIT,DIEP FLAP , Catalog Number:PB23DFCM5; 4) KIT,DIEP FLAP , Catalog Number:PB23DFCM6; 5) KIT,DIEP FLAP , Catalog Number:PB23DFCM7; 6) KIT,DIEP FLAP , Catalog Number:PB23DFCMA; 7) KIT, HEAD AND NECK , Catalog Number:PE40HNAJ10; 8) KIT, HEAD AND NECK , Cata
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
- 2025-02-13CPSCDMITOY, of China6-in-1 Pounding Games Recalled Due to Ingestion Hazard; Violation of Federal Regulations for Magnets; Sold Exclusively on Temu.com by DMITOY
The recalled 6-in-1 Pounding Game violates the mandatory federal regulation for magnets because it contains a magnet that can become loose, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.
- 2025-02-12FDA-FoodAtkinson Milling CompanyClass IATKINSON'S NO ONIONS PLAIN NO ONIONS HUSHPUPPIES NET WT. 2 LB. 8 OZ. UPC 0 72119 20304 7 Ingredients: Enriched Whole Grain Corn Meal***Enriched Wheat Flour, Sugar, Onions, Salt, Eggs, Sodium Bicarbonate Sodium Aluminum Phosphate, Acidic Monocalcium Phosphate and Natural Flavors. Contains: Wheat, Eggs, Soy. Atkinson Milling Company, Inc. 95 Atkinson Mill Road Selma, NC 27576
Undeclared Milk. During the firm's reordering process of labels, they discovered that the label does not list milk in its ingredient or contain statement.
- 2025-02-12FDA-FoodAtkinson Milling CompanyClass IATKINSON'S HUSHPUPPIES WITH ONIONS NET WT. 1LB. (454 g) UPC 0 72119 20718 2 and NET WT. 2 LB. 8 OZ. UPC 0 72119 20305 4 Ingredients: Enriched Whole Grain Corn Meal***Enriched Wheat Flour, Sugar, Onions, Salt, Eggs, Sodium Bicarbonate Sodium Aluminum Phosphate, Acidic Monocalcium Phosphate and Natural Flavors. Contains: Wheat, Eggs, Soy. Atkinson Milling Company, Inc. 95 Atkinson Mill Road Selma, NC 27576
Undeclared Milk. During the firm's reordering process of labels, they discovered that the label does not list milk in its ingredient or contain statement.
- 2025-02-06CPSCRainbow Trade (HK) Co. Limited, of Hong KongUVIPC Baby Gates Recalled Due to Entrapment Hazard; Violation of Federal Regulations for Gates and Enclosures; Sold Exclusively on Amazon.com by Xianshengyouli
The recalled baby gates violate the federal safety regulations for expansion gates and expandable enclosures. For the versions with a pet door, a child's torso can fit through the secondary opening and, for the other versions that are adjustable, a child's torso can fit through the opening between the gate slat and side wall. These violations pose an entrapment hazard to children.
- 2025-02-06CPSCDoosan Bobcat North America, of West Fargo, North DakotaDoosan Bobcat North America Recalls Bobcat & Steiner AirFX Finish Mower Deck Attachments Due to Crush Hazard
The recalled mower decks cannot be secured in the upright or tilted position by the locking pins during maintenance or service, posing a crush hazard.
- 2025-01-29FDA-FoodMR BING FOODS INC.Class IIMr. Bing brand Sriracha Chili Sauce; 9 oz and 18 oz, in clear PET bottle with green cap; UPC 850044819072 and UPC 850044819058
Product may contain spoilage organisms.
- 2025-01-22FDA-DeviceAugustine Temperature Management, LLCClass IIAugustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) WC77V; 2) WC77V-DEMO; 3) WC77V-R; used in conjunction with Warming Blankets and Mattresses, veterinary use.
HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
- 2025-01-22FDA-DeviceAugustine Temperature Management, LLCClass IIAugustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) WC71V; 2) WC71V-DEMO; 3) WC71V-R; used in conjunction with Warming Blankets and Mattresses, veterinary use.
HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
- 2025-01-22FDA-DeviceAugustine Temperature Management, LLCClass IIHillrom Temperature Management Controller, MP, Model # 2083516; used in conjunction with Warming Blankets and Mattresses.
HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
- 2025-01-22FDA-DeviceAugustine Temperature Management, LLCClass IIAugustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) Model # WC77, 2) Model # WC77D (Demo), 3) Model # WC77R (Refurbished); used in conjunction with Warming Blankets and Mattresses.
HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
- 2025-01-22FDA-DeviceAugustine Temperature Management, LLCClass IIAugustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) Model # WC71, 2) Model # WC71R (refurbished); used in conjunction with Warming Blankets and Mattresses.
HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
- 2024-12-25FDA-DeviceAugustine Temperature Management, LLCClass IIHillrom Temperature Management Controller, MP, Model # 2083516; used in conjunction with Warming Blankets and Mattresses.
Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to Power-on self-test error code "EA POST".
- 2024-12-25FDA-DeviceAugustine Temperature Management, LLCClass IIAugustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Multiport, Models: 1) Model # WC77, 2) Model # WC77D (Demo), 3) Model # WC77R (Refurbished); used in conjunction with Warming Blankets and Mattresses.
Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to Power-on self-test error code "EA POST".
- 2024-12-25FDA-DeviceAugustine Temperature Management, LLCClass IIAugustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) Model # WC71, 2) Model # WC71R (refurbished); used in conjunction with Warming Blankets and Mattresses.
Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to Power-on self-test error code "EA POST".
- 2024-12-19CPSCMelii Baby Inc., of CanadaMelii Baby Silicone Spoons for Babies Recalled Due to Choking Hazard; Imported by Melii Baby
The silicone spoon can break apart while in use, posing a choking hazard to babies.
- 2024-12-18FDA-FoodDeseret Biologicals IncClass IIDesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, 30 count in a Blue PET bottle with a White cap. Supplement facts declare Phosphatidylserine (from non-GMO sunflower lecithin powder) 40 mg. Distributed by Deseret Biologicals Inc 469 West Parkland Dr, Sandy, UT.
Product contains undeclared soy lecithin.
- 2024-12-05CPSCPolaris Industries Inc., of Medina, MinnesotaPolaris Recalls Ranger Recreational Off-Road Vehicles and ProXD and Bobcat Utility Task Vehicles Due to Injury Hazard (Recall Alert)
The vehicles' passenger side seat belt anchor point can separate from the frame due to a defective weld on the bracket, posing an injury hazard to passengers from impact with a loose bracket or failure of the seatbelt during a crash.
- 2024-12-04FDA-DeviceRemote Diagnostic Technologies Ltd.Class IIITempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode
Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.
- 2024-12-04FDA-DeviceDefibtech, LLCClass IIDefibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, Lifeline ECG, Lifeline View (DDU-2XXX Series -Indicated for use on victims of sudden cardiac arrest (SCA.)
Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient
- 2024-12-04FDA-DeviceDefibtech, LLCClass IIDefibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DDU-2XXX Series). -Indicated for use on victims of sudden cardiac arrest (SCA.)
Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient
- 2024-12-04FDA-DeviceDefibtech, LLCClass IIDefibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victims of sudden cardiac arrest (SCA.)
Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient
- 2024-12-04FDA-DeviceDefibtech, LLCClass IIDefibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of sudden cardiac arrest (SCA)
Within the Irish Market, a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life. There is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient.
- 2024-11-13FDA-DeviceCanon Medical System, USA, INC.Class IICartesion Prime, Digital PET-CT, Model: PCD-1000A/3D.004, PCD-1000A/3D, is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems.
When PET-CT system is executing reconstruction, if PET acquisition for another patient is performed (or PET reconstruction for another patient is performed from raw data processing), PET reconstruction control processing may hang up and PET reconstruction may stop as a result, which may necessitate repeat PET/CT examinations.
- 2024-11-13FDA-FoodPerfection Bakeries LLCClass IAunt Millie s Bakehouse Whole Grain White Hot Dog Buns 6" Sliced 2 OUNCE. 12 unlabeled 12CT PKGS per sale unit case, product code 7502. Net. Wt. 18lbs.
Undeclared sesame
- 2024-11-06FDA-FoodGlaser Organic FarmsClass IIAll Raw Vegan Certified Organic Salsa, Glaser Organic Farms, Handmade fresh from our farm to you,Net wt. 8 oz, Plastic PET Container with cover, Keep Refrigerated, UPC 832910 001514
Product may contain Foreign object: Glass
- 2024-10-30FDA-DeviceMEDLINE INDUSTRIES, LP - NorthfieldClass IIMedline brand medical procedure convenience kits, labeled as: 1) EYE PACK, REF DYNJ19492L; 2) PHACO PACK, REF DYNJ22354L; 3) EYE PACK, REF DYNJ24573K; 4) EYE PACK, REF DYNJ30327A; 5) BASIC CATARACT PACK, REF DYNJ36868F; 6) BASIC RETINA PACK, REF DYNJ40811A; 7) OPHTHALMOLOGY PACK CKHA-LF, REF DYNJ41769A; 8) CATARACT PACK WRO-LF, REF DYNJ41861; 9) EYE PACK, REF DYNJ43911; 10) PHACO PACK, REF DYNJ44748I; 11) DR DRUMMOND EYE PACK, REF DYNJ45344G; 12) OPHTHALMIC PACK, REF DYNJ47275A; 13
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
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