Pet food and pet product recalls
1081 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.
- 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.
- 2024-10-17CPSCTextron Specialized Vehicles, of Augusta, GeorgiaTextron Specialized Vehicles Expands Recall of Arctic Cat and Tracker Side by Side Recreational Off Highway Vehicles Due to Crash Hazard (Recall Alert)
The vehicle can move when on an incline and "park" is displayed on the digital dash. This can allow the vehicle to roll away, posing a crash hazard.
- 2024-10-10CPSCFisher-Price of East Aurora, New YorkFisher-Price Recalls More than 2 Million Snuga Infant Swings Due to Suffocation Hazard After 5 Deaths Reported
The swing should never be used for sleep and bedding materials should never be added to it. If the product is used for sleep or bedding material is added, the headrest and body support insert on the seat pad can increase the risk of suffocation.
- 2024-10-10CPSCShenzhen Jingdu Technology Co. Ltd., of ChinaGimars Playpens Recalled Due to Entrapment and Suffocation Hazards; Violation of Federal Regulations for Play Yards; Imported by Shenzhen Jingdu Technology and Sold Exclusively on Amazon.com
The recalled playpens violate the federal safety regulations for play yards. The included basketball hoop accessory can be a head entrapment hazard and children can become entrapped beneath the mattress, posing a suffocation hazard.
- 2024-09-11FDA-FoodRefresco Beverages US IncClass IIa.) Great Value 8oz Apple Juice in 6pack; PET plastic bottle b.) Great Value 96oz Apple Juice; PET plastic bottle c.) Market Basket 100% apple juice; 64 oz; PET plastic bottle d.) Nice! 100% apple juice ; 64 oz; PET plastic bottle e.) Weis 100% apple juice; 64 oz; PET plastic bottle f.) Urban Meadow 100% apple juice; 64 oz; PET plastic bottle g.) Natures Nectar 100% apple juice; 64 oz; PET plastic bottle h.) Wellsley Farms 100% apple juice; 96 oz; PET plastic bottle i.) Solevita 100% app
Products contains inorganic arsenic above action level set in guidance to industry.
- 2024-09-04FDA-FoodAmerican Spice LLCClass IISpice Class brand Ground Cinnamon packed in 7oz and 11oz PET jars
Product contains elevated levels of lead (2,040ppb).
- 2024-08-28FDA-FoodRefresco Beverages US IncClass IIGreat Value; 8oz Apple Juice in 6 pack; 100% Juice; packaged in 8 oz. PET plastic bottles; UPC 0-78742-29655-5
Product contains inorganic arsenic above action level set in industry guidance (13.2ppb)
- 2024-08-15CPSCHangzhoumeixiajianzhushejiyouxiangongs D/B/A MEIXIA Shop, of ChinaMamibaby and Cosy Nation Baby Loungers Recalled Due to Suffocation Risk and Fall and Entrapment Hazards; Violation of Federal Regulations for Infant Sleep Products; Sold on Amazon.com by MEIXIA Shop and Softbless
The recalled baby loungers violate the federal safety regulations for Infant Sleep Products because the sides are too low to contain the infant; the sleeping pad is too thick, posing a suffocation hazard; an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped; and the loungers do not have a stand, posing a fall hazard if used on elevated surfaces. These violations create an unsafe sleeping environment for infants.
- 2024-07-25CPSCTextron Specialized Vehicles, of Augusta, GeorgiaTextron Specialized Vehicles Recalls 2024 Arctic Cat Mountain 600 Snowmobiles Due to Crash Hazard
The pin on the u-joint of the steering knuckle was not swagged correctly, which can allow the pin to come out of the u-joint and cause the rider to lose steering control, posing a crash hazard.
- 2024-07-25CPSCOphanie, of ChinaOphanie Area Rugs Recalled Due to Fire Hazard; Violation of Federal Flammability Regulations; Sold Exclusively on Amazon.com by Ophanie
The recalled area rugs violate the mandatory federal flammability regulations for carpets and rugs, posing a fire hazard.
- 2024-07-24FDA-DeviceB. Braun Medical, Inc.Class IIInfusomat UNIV. 15 DROP PUMP SET W/3 SAFELINE, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363030
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.
- 2024-07-24FDA-DeviceB. Braun Medical, Inc.Class IIInfusomat 60DROP METRISET PUMP SET, 3 SAFELINE-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362034
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.
- 2024-07-24FDA-DeviceB. Braun Medical, Inc.Class IIInfusomat UNIV.15DROP PUMP SET W/3 SAFELINE LL-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362032
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.
- 2024-07-24FDA-DeviceGreiner Bio-One North America, Inc.Class IIVACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged
The firm received reports that some blood collection tubes have experienced issues with clotting and poor separation due to missing additive. The failure of the device would likely require sample recollection which could result in a delay of treatment.
- 2024-07-24FDA-FoodSnapchill, LLCClass IIBlack Coffee Canned Beverage packaged under the following brands and sizes: 1. 41 & Change Coffee Co A Finca / Nicaragua Cold Coffee, 12 oz. UPC 1 97644-95863 4. 2. Alchemy Roast Elixir or Life (Gutemala/Huehuetenango Blend) 12 oz. UPC 8 10149-37056 4. 3. Amavida Coffe Roasters Guatemala Manos Campesinas, 12 oz. UPC 8 10149-37046 5. 4. Appalachia Coffee Nitro Cold Coffee Kentucky Black Gold, 12 oz. UPC 8 10149-37091 5. 5. Baba Java Coffee Roasters Ridge Blend (Ethiopian/Honduras) 12
Potential under-processing.
- 2024-07-10FDA-FoodBreadbox Co.Class IIBreadman Brioche products in plastic bags: Brioche Toast, 2 lb. (1 loaf/bag), Brioche Buns, 40oz (10 buns/bag), Brioche Sliders, 50oz (25 sliders/bag), Brioche Hot Dog, 40oz (10 buns/bag)
Undeclared Yellow No. 5
- 2024-07-10FDA-FoodPenn Herb Company, Ltd.Class INature's Wonderland brand Thyroid Formula 60 Veg Capsules UPC: 715486893205. Packaged in White PET 150cc bottle with security closure
Potential Salmonella contamination
- 2024-07-03FDA-FoodClassic Delight LLCClass II(Item 7060) Classic Delight Chili Cheese Dogs
Possibly contaminated with Listeria monocytogenes
- 2024-06-20CPSCBabboe B.V., of the NetherlandsCargo Bicycles Recalled Due to Fall Hazard; Manufactured by Babboe B.V.
The frames of the recalled cargo bicycles can crack and can bend and break, posing a fall hazard to the rider.
- 2024-06-06CPSCSpectrum Brands Pet LLC, of Middleton, WisconsinSpectrum Brands Pet Care Recalls Pet Fur deShedding Conditioner Due to Risk of Exposure to Bacteria
The recalled conditioner can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.
- 2024-06-06CPSCKawasaki Motors Manufacturing Corp. U.S.A., of Maryville, MissouriKawasaki Motors USA Recalls Engines Used in Bad Boy Mowers, BigDog, Bobcat, Cub Cadet, Hustler, John Deere and Kubota Brand Lawn and Garden Equipment Due to Fire and Burn Hazards
The recalled engines can overheat, posing fire and burn hazards.
- 2024-06-05FDA-DeviceMEDLINE INDUSTRIES, LP - NorthfieldClass IIMedline medical procedure kits, labeled as follows: a) PARACERVICAL PUD TRAY, REF DYNDH1832; b) AHS PARACERVICAL/PUDENDAL KIT, REF DYNJRA2210; c) PARACERVICAL/PUDENDAL BLK KIT, REF DYNJRA9046; d) PARACERVICAL/PUDENDAL BLK KIT, REF DYNJRA9046H; Medical procedure convenience tray
Trumpet Needle Guide ring can detach when excessive pressure is applied.
- 2024-06-05FDA-DeviceMEDLINE INDUSTRIES, LP - NorthfieldClass IICenturion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray
Trumpet Needle Guide ring can detach when excessive pressure is applied.
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