Pet food and pet product recalls
1082 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.
- 2015-07-29FDA-DevicePhilips Medical Systems (Cleveland) IncClass IIGEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Imaging Systems are a family of integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) systems suitable for a wide range of diagnostic applications.
Philips has identified four (4) software defects in the Tumor LOC software application that may potentially result in irradiation of healthy tissue or non-irradiation of diseased tissue.
- 2015-07-29FDA-DeviceHardy DiagnosticsClass IIHardyCHROM VRE Agar-RSR Cat no: GA333 Lot no: H15055 Expires: 2015-07-04 Container type: 15x100mm monoplate Packaged: 10 plates/sleeve Storage 2 to 8 degrees C on receipt Chromogenic medium for stool pathogen screening.
Hardy Diagnostics is recalling HardyCHROM VRE Agar due to lack of 510(k) clearance.
- 2015-07-28CPSCArctic Cat Inc., of Thief River Falls, Minn.Arctic Cat Recalls Off-Highway Utility Vehicles Due to Fuel Leak and Fire Hazard (Recall Alert)
Fuel can leak from the fuel fitting at the throttle body, posing a fire hazard.
- 2015-07-28CPSCKyber Outerwear USA Corp., of Ogdensburg, NYKyber Outerwear Recalls Children’s Sweaters Due to Strangulation Hazard
The sweaters have a drawstring around the neck area that poses a strangulation hazard to children. Drawstrings can become entangled or caught on playground slides, hand rails, school bus doors or other moving objects, posing a significant strangulation and/or entanglement hazard to children.
- 2015-07-22FDA-FoodProject 7Class IISour Caramel Apple Chewing, net wt .53 oz, Gum UPC 844911 002919. Sour Caramel Apple chewing gum tablet packed in 12ct metalized PET Pouch with zipper.
Project 7 is recalling all lots of Sour Caramel Apple Chewing Gum because the caramel flavoring ingredient in the gum contains undeclared milk.
- 2015-07-16USDAClass IIICheck The Sausage Factory sausage packages for USDA seal
Misbranding
- 2015-07-01FDA-FoodCoca-Cola Company (The)Class IIDiet Dr. Pepper, 8 x 12 fl. oz. PET bottle, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 85024.
A Diet Dr. Pepper labeled product contain regular Dr. Pepper.
- 2015-07-01FDA-DrugBracco Diagnostic IncClass IIIE-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing), 23 g foil pouches, Rx only, Manufactured by E-Z-EM Canada Inc. a subsidiary of E-Z-EM Inc., Lake Success NY NDC 32909-727-01
Failed stability specifications:This recall has been initiated due to out of specification results for viscosity.
- 2015-06-17FDA-DeviceBecton Dickinson & Co.Class IIBBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.
The products may exhibit indications of excessive oxidation. Excessive oxidation may affect the viability of anaerobic microorganisms.
- 2015-06-17FDA-DeviceBecton Dickinson & Co.Class IIBBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials contain a reduced transport medium and are intended to maintain the viability of anaerobic, facultative and aerobic microorganisms during transport from the patient to the laboratory. Sterile packages are for collection of specimens in clean areas; e.g., surgical suites.
The products may exhibit indications of excessive oxidation. Excessive oxidation may affect the viability of anaerobic microorganisms.
- 2015-06-16CPSCBunnies by the Bay of East Windsor, N.J.Bunnies by the Bay Recalls Pull Toys Due to Choking Hazard
Hub caps on the wheels can break or come off the wheel, posing a choking hazard for young children.
- 2015-04-22FDA-DeviceHardy DiagnosticsClass IIHardy Diagnostics cat no. G327 HardyCHROM SS Agar (HardyCHROM Salmonella Shigella) Cat no: G327 Container type: 15x100mm monoplate Packaged: 10 plates/sleeve Storage: 2 to 8 degrees C. on receipt in dark A selective chromogenic medium for the primary screening isolation, and differentiation of Salmonella & Shigella spp.
The firm is recalling HardyCHROM SS, Cat. no. G327 Lot no. 15037 due to a report of possible lack of color development in Shigella organisms in the referenced lot.
- 2015-04-16CPSCGoochie Goo Garbs LLC, of Scottsdale, Ariz.Goochie Goo Garbs Recalls Children's Sensory Grab Garb Blankets Due to Laceration Hazard
Wire-edged ribbon used in the blanket's ribbon tags can become exposed, posing a laceration hazard to children.
- 2015-04-15FDA-DrugWallcur IncorporatedClass IPracti-0.9% Sodium Chloride, 50 mL, 100 mL, 250 mL, 500 mL, and 1000 mL bags, Product of China, Wallcur, San Diego, CA, 92111, USA; Wallcur Practi Products for Clinical Simulation; NDCs 5108-0954-75, 5108-0954-71, 5108-0954-72, 5108-0954-74, 5108-0954-73.
Non-sterility: Product is made in a non-sterile facility and is not intended for use in humans or animals.
- 2015-03-20USDAClass IDon't eat NOBRE Receitas Caseiras canned meat
Import Violation
- 2015-03-11FDA-DeviceXoran Technologies, LLCClass IIXoran MiniCAT X-ray imaging device
Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose.
- 2015-02-19USDAClass IKenosha Beef International Recalls Beef Product Due to Possible Listeria Contamination
Product Contamination
- 2015-02-04FDA-FoodSunBurst Foods, Inc.Class ISingle Hot Dog w/Chili, Net Wt., 3.10 oz., UPC 7-01248-00800-0, MFG Code 285
Listeria monocytogenes
- 2015-01-28USDAClass IDon't use Washington Beef trim product
Product Contamination
- 2014-12-31FDA-FoodCoca-Cola Company (The)Class IIICoca Cola Zero, 2 liter pet bottle, UPC 49000 05014, The Coca Cola Company
Equipment malfunction led to ingredients to be blended at levels that are inconsistent with approved formulations.
- 2014-12-17FDA-DeviceSkeletal DynamicsClass IIAlign Radial Stems, Prosthesis, Elbow, Hemi Replacement of the radial head for degenerative or post-traumatic disabilities presenting pain, crepitation, and decreased motion at the radio-humeral and/or proximal radio-ulnar joint with: Joint destruction and/or subluxation and resistance to conservative treatment. Intended use is also for primary replacement after fracture of the radial head and symptomatic sequelae after radial head resection.
Report received where the Align Radial Stem fractured.
- 2014-11-26FDA-DeviceSiemens Healthcare Diagnostics, IncClass IIIADVIA Centaur BNP Assay for in vitro diagnostic use in the quantitative determination of B-type Natriuretic Peptide (BNP) in human plasma using the ADVIA Centaur, Centaur XP, Centaur CP Systems; Catalog Numbers: Cat No. 02816138/SMN 10309044 (100 test) 02816634/SMN 10309045 (500 test)
Siemens Healthcare Diagnostics has confirmed that approximately 2000 ReadyPacks from the ADVIA Centaur¿ Systems BNP reagent contains an ADVIA Centaur Systems FT4 human-readable side label.
- 2014-11-20CPSCSchiller Grounds Care, Inc., of Johnson Creek, Wisc.Bob-Cat Recalls Zero Turn Mowers Due to Crash Hazard (Recall Alert)
The steering control arm component can break under normal use, causing driver to lose control and crash.
- 2014-11-18CPSCBlack Diamond Inc., of Salt Lake CityBlack Diamond Equipment Recalls Whippet Ski Poles Due to Risk of Injury
The stainless steel pick in the handgrip can break and fail to slow or stop users from sliding downhill on a snow or ice covered slope, posing a risk of injury.
- 2014-11-18USDAClass IDo not eat pretzel dogs with soy allergen
Misbranding, Unreported Allergens
- 2014-11-15USDAClass IReturn pretzel dogs with soy allergen
Misbranding, Unreported Allergens
- 2014-10-29FDA-DeviceDeRoyal Industries IncClass IIDeRoyal(R) SafeLiner Suction Canister Kit, SEMI-RIGID, 1000cc, REF 71-6518, NON-STERILE, Rx Only, general hospital
These lots of suction canisters and lids have an insufficient seal under low or intermittent suction condition.
- 2014-10-23CPSCArctic Cat Inc., of Thief River Falls, Minn.Arctic Cat Recalls Single-Rider and 2UP ATVs Due To Crash Hazard
Components in the front gear case can fail, posing a risk of loss of control and crash hazard.
- 2014-10-15FDA-DeviceBiomedix, Inc.Class IIBiomedix SELEC-3 I.V. Administration Set. Individually sealed into a Tyvek¿ and LDPE/PET pouch. Secondary packaging includes 48 pouched units per box/case. STERILE
Customer contacted Biomedix of complaint and returned the failed set along with 86 units of unopened stock (96 units originally shipped). Biomedix performed extensive investigation and found insufficient application of glue. Recall was initiated due to the rate of the failure.
- 2014-09-24FDA-DeviceGenesis BPS, LLC.Class IIPedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS, LLC The intended use is to prepare and deliver small aliquots of filtered whole blood, red blood cells, platelets, plasma, and cryoprecipitate for pediatric and or neonatal transfusion.
Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.
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