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.
- 2019-04-18CPSCArctic Cat Inc., of Thief River Falls, Minn.Arctic Cat Recalls Snowmobiles Due to Fire Hazard (Recall-Alert)
While operating the snowmobile the exhaust can flame from the muffler outlet, posing a fire hazard.
- 2019-03-28CPSCMidwest-CBK, LLC, of Cannon Falls, Minn.Midwest-CBK Recalls Baby Rattle Socks Due to Choking Hazard
Small ornaments can detach from the socks, posing a choking hazard to young children.
- 2019-03-27FDA-DeviceAgfa N.V.Class IIIPET Plates Coated Film-MONOMEDBV2S2- Radiographic Film REF: XJUB8, XJM73, XJUDD, XJM85, EKLYZ. Product Usage: Due to an inhomogeneous coating solution, pinholes can become visible in even dark images. Visibility of the pinholes varies as material from this coating run shows pinholes in different frequencies and intensities.
Due to an inhomogeneous coating solution, pinholes can become visible in even dark images. Visibility of the pinholes varies as material from this coating run shows pinholes in different frequencies and intensities
- 2019-03-26CPSCYiwu City Fuman Leather & Accessories Co., Ltd., of ChinaRechargeable Power Banks Recalled by Daniel M. Friedman & Associates Due to Fire Hazard
The power banks can overheat, posing a fire hazard
- 2019-03-20FDA-DrugKing Bio Inc.Class IDr. King's SafeCare Rx Allergies Animal Hair & Dander Allergy, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955219620, NDC 57955-2196-2
Microbial contamination
- 2019-03-20FDA-DrugKing Bio Inc.Class IDr. King's Natural Medicine Homeopathic Animal Hair & Dander Allergy Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955519621, NDC 57955-6490-2
Microbial contamination
- 2019-03-08CPSCThe TJX Companies Inc., of Framingham, Mass.TJX Recalls Heating Pads Due to Fire and Burn Hazards; Sold Exclusively at T.J. Maxx and Marshalls Stores
The heating pads can overheat during use, posing fire and burn hazards.
- 2019-03-05CPSCArctic Cat Inc., of Thief River Falls, Minn., a subsidiary of Textron Specialized Vehicles, of Augusta, GaArctic Cat Recalls Textron Off-Highway Utility Vehicles Due to Crash Hazard (Recall Alert)
The lower front suspension arm can fail, posing a crash hazard.
- 2019-03-05CPSCArctic Cat Inc., of Thief River Falls, Minn., a subsidiary of Textron Specialized Vehicles, of Augusta, Ga.Arctic Cat Recalls Textron Off-Highway Utility Vehicles Due to Fuel Leak and Fire Hazard (Recall Alert)
Fuel can leak from the fuel line, posing a fire hazard.
- 2019-02-27FDA-DeviceLeica Microsystems, Inc.Class IIPROVEO 8 Ophthalmic Microscope System optical instrument for improving the visibility of objects through magnification and illumination. It can be applied for observation and documentation and for human and veterinary medical treatment.
The observed issues can lead to unexpected interruptions of the optics carrier focus drive movement, intermittent stops of the X-Y coupling movement or sporadic failures in the proper on-screen display functionality of the HDR recording unit. Additionally, an anomaly in the device software may also lead to the unexpected behavior that when a user releases a handle or foot switch button this may not immediately end the actuated functionality. This behavior can only occur in unlikely workflows where a user changes a user profile or a mode change is initiated at the same time as a functional button is activated.
- 2019-02-27FDA-FoodSysco CharlotteClass IIDannon YOGURT STWBRY DANIMAL CRSH
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
- 2019-02-22USDAClass IDon't eat Golden Boy frozen catfish
Produced Without Benefit of Inspection
- 2019-02-20FDA-DevicePhilips Medical Systems (Cleveland) IncClass IIIngenuity TF PET/CT (non-RoHS), Model Number 882456 This device is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem produces cross-sectional images of the body by computer reconstruction of x-ray transmission data. The PET subsystem produces images of the distribution of PET radiopharmaceuticals in the patient body (specific radiopharmaceuticals are used for whole body, brain, heart and other organ imagin
A software update is being issued to correct multiple issues identified in the previous software version.
- 2019-02-12CPSCPutian Licheng Phoenix Footwear CO., of Fujian, ChinaTarget Recalls Toddler Boots Due to Choking Hazard
The unicorn horn on the boot can detach, posing a choking hazard to children.
- 2019-01-30FDA-DeviceLeica Microsystems, Inc.Class IILeica M220 F12 surgical microscope The Leica M220 F12 surgical microscope is an optical instrument for improving the visibility of objects through magnification and illumination. It can be applied for observation and documentation and for human and veterinary medical treatment.
The M220 optics may unintentionally drop into the surgical field, risking contact with the patient.
- 2019-01-09FDA-DeviceORTHO-CLINICAL DIAGNOSTICSClass IIVITROS NT-proBNP Reagent, Cat No. 6802156 Product Usage: For in vitro diagnostic use only. For the quantitative measurement of N-terminal pro Brain Natriuretic Peptide (NT-proBNP) in human serum and plasma (EDTA or heparin) using the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System to aid in the diagnosis of congestive heart failure and for the risk stratification of acute coronary syndrome and congestive heart failure. T
The firm is extending their previous July 2018 recall to include additional product codes. Biased results may occur for these additional products at biotin concentrations which are lower than indicated in the current Instructions for Use.
- 2019-01-09FDA-DeviceORTHO-CLINICAL DIAGNOSTICSClass IIVITROS Anti-HBe Reagent Pack, Cat No. 6801816 Product Usage: For the in vitro qualitative detection of antibodies to hepatitis B e antigen (anti-HBe) in human adult and pediatric (2 to 21 years old) serum from individuals who have symptoms of chronic hepatitis and those who have recovered from HBV infection, using the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System. Further assessment of HBV infection (biochemical, serol
The firm is extending their previous July 2018 recall to include additional product codes. Biased results may occur for these additional products at biotin concentrations which are lower than indicated in the current Instructions for Use.
- 2018-12-26FDA-DeviceCOVIDIEN LLCClass II8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve), Model Number 36826
The product was released into commercial distribution while subject to importation refusal.
- 2018-12-19FDA-DeviceAngiodynamics Inc. (Navilyst Medical Inc.)Class IIXcela Power Injectable PICC with PASV (XCELA PASV 4F SL 55CM Catheter Kit CE PG), Cat no. 55-711
Specific lots of Xcela Power Injectable and BioFlo PICCs are labelled with incorrect expiration dates. The labelled expiration date extends the shelf life of the product beyond the date supported by validation testing. Although the product under recall has not yet reached its validated expiry date, removal of the affected product is warranted to prevent use beyond the validated expiry date.
- 2018-11-28FDA-FoodLehi Valley Trading Co.Class IIMast Store Provisioners, Animal Crackers, Net Wt. 8 OZ. clear plastic bag
The firm noticed that multiple snack food items for a customer had the same information panel. Therefore the ingredient list and allergen information is incorrect.
- 2018-11-07FDA-DevicePhilips Medical Systems (Cleveland) IncClass IIVereos PET/CT, Software version 2.0.1. Model Number: 882446 Product Usage: The Philips Vereos PET/CT system is a diagnostic imaging device that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem images anatomical cross-sections by computer reconstruction of X-ray transmission data. The PET subsystem images the distribution of PET anatomy-specific radiopharmaceuticals in the patient. The PET/CT system is used for the purposes of detecti
Software Correction: Software errors that may result in incorrect 4D CT images, PET images with SUV quantification error, or disruption of interventional CT procedures; and Software errors that may result in partial set of images, inability to generate CT or PET images, incorrect scan parameters, or scanning the incorrect portion of the body.
- 2018-10-24FDA-DeviceSiemens Healthcare Diagnostics, IncClass IIAtellica IM CKMB Master Curve Material, Cat No. 10995534 Product Usage: For in vitro diagnostic use for evaluating the ADVIA Centaur CKMB assay. This material is intended to be run singly as unknown samples after a two-point calibration has been performed on the system.
A potential bias was identified with certain kits compared to the internal standards.
- 2018-10-24FDA-DeviceSiemens Healthcare Diagnostics, IncClass IIAtellica IM CKMB Calibrator, Cat No. 10995532 Product Usage: For in vitro diagnostic use for evaluating the ADVIA Centaur CKMB assay. This material is intended to be run singly as unknown samples after a two-point calibration has been performed on the system.
A potential bias was identified with certain kits compared to the internal standards.
- 2018-10-24FDA-DeviceSiemens Healthcare Diagnostics, IncClass IIADVIA Centaur CKMB Master Curve Material, Cat No. 07867768 Product Usage: For in vitro diagnostic use for evaluating the ADVIA Centaur CKMB assay. This material is intended to be run singly as unknown samples after a two-point calibration has been performed on the system.
A potential bias was identified with certain kits compared to the internal standards.
- 2018-10-24FDA-DeviceSiemens Healthcare Diagnostics, IncClass IIADVIA Centaur CKMB Calibrator 2-pack Japan, Cat No. 02562748 Product Usage: For in vitro diagnostic use in calibrating ADVIA Centaur systems CKMB assays.
A potential bias was identified with certain kits compared to the internal standards.
- 2018-10-24FDA-DeviceSiemens Healthcare Diagnostics, IncClass IIADVIA Centaur CKMB Calibrator, Cat No. 09318028 Product Usage: For in vitro diagnostic use in calibrating ADVIA Centaur systems CKMB assays.
A potential bias was identified with certain kits compared to the internal standards.
- 2018-10-17FDA-DeviceBayer Medical Care, Inc.Class IICodan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion Systems Product Usage: 1.2 micron filter for use with Intravenous Administration Sets
Bayer has received reports of loose particulate in the filter when the dust cap is removed. Bayer conducted further testing confirming the dust cap may generate particulate which may potentially enter the fluid path.
- 2018-10-10USDAClass IDo not eat Malone's Fine Sausage pork head cheese
Product Contamination
- 2018-09-05FDA-DeviceStryker Leibinger GmbH & Co. KGClass IIAXS PP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01541S, for use on the cranium
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
- 2018-09-05FDA-DeviceStryker Leibinger GmbH & Co. KGClass IIAXS PP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01540S, for use on the cranium
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
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