Pet food and pet product recalls
1069 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.
- 2015-04-15FDA-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.
- 2014-09-24FDA-DeviceGenesis BPS, LLC.Class IIPedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/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.
- 2014-09-24FDA-DeviceGenesis BPS, LLC.Class IIPedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson 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.
- 2014-09-24FDA-DeviceAmerx Health Care Corp.Class IIAmerigel Daily Dressing Advanced 3-in-1 Hydrogel; 30 single used foil packets 1g. each; CAT # A2003. Wound management.
Not approved labeling claims (antimicrobial and autolytic debridement)
- 2014-09-24FDA-DeviceAmerx Health Care Corp.Class IIAmerigel Post-Op Surgical Kits . Kit includes: Amerigel Wound Dressing, Amerigel Wound Wash, 22x2 Gauze Pads, and 1x3 Fabric Bandages CAT # A2002. Wound management.
Not approved labeling claims (antimicrobial and autolytic debridement)
- 2014-09-24FDA-DeviceAmerx Health Care Corp.Class IIAmerigel Hydrogel Saturated Gauze Dressing; 10 Individually Packaged pads size 2x2 4 Ply Pads; CAT # A5002. Wound management.
Not approved labeling claims (antimicrobial and autolytic debridement)
- 2014-09-23USDAClass IDon't eat Applegate Naturals beef corn dogs
Processing Defect
- 2014-09-11CPSCArctic Cat, Inc., of Thief River Falls, Minn.Arctic Cat Recalls Side by Sides Due to Fire Hazard (Recall Alert)
Oil can leak from the oil cooler lines, posing a fire hazard.
- 2014-09-10FDA-DeviceCustomed, IncClass ILAPAROSCOPY COLORECTAL SURGICAL PACK code 900-2259A, contains: (1) SOLUTION SURGICAL DURAPREP 26ml LIF (4) DRAPE UTILITY WITH TAPE LIF (3) TOWELS ABSORBENT 15" X 20" LIF (2) LEGGINS W/7'' CUFF 30" X 42" LIF (1) BLADE SURGICAL# 15 STAINLESS STEEL (1) BLADE SURGICAL# 11 STAINLESS STEEL (1) GOWN IMPERV. EXTRA REINF. XLG AAMI Il l LIF (1) IRRIGATION SUCTION TROMPET DUAL SPIKE LIF (1 0) GAUZE SPONGE 4" X 4" 16PL Y XRD LIF (2) UTILITY BOWL 16oz. LIF (2) PK. STERI STRIP CLOSURE%'' X 4" L/F
Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.
- 2014-09-10FDA-DeviceCustomed, IncClass ILAPAROSCOPY COLORECTAL SURGICAL PACK CONTENTS: (1) SOLUTION SURGICAL DURAPREP 26ml LIF (4) DRAPE UTILITY WITH TAPE LIF (3) TOWELS ABSORBENT 15" X 20" LIF (2) LEGGINS W/7'' CUFF 30" X 42" LIF (1) BLADE SURGICAL# 15 STAINLESS STEEL (1) BLADE SURGICAL# 11 STAINLESS STEEL (1) GOWN IMPERV. EXTRA REINF. XLG AAMI Ill LIF (1) IRRIGATION SUCTION TROMPET DUAL SPIKE LIF (10) GAUZE SPONGE 4" X 4" 16PLY XRD LIF (2) UTILITY BOWL 16oz. LIF (2) PK. STERI STRIP CLOSURE%'' X
Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.
- 2014-09-10FDA-DeviceCustomed, IncClass ILAPAROSCOPIA COLORECTAL PACK CONTENTS: (1) SOLUTION SURGICAL DURAPREP 26ml (4) DRAPE UTILITY WITH TAPE (1) TOWELS ABSORBENT 15" X 20" (2) LEGGINS W/7" CUFF 30" X 42" (1) BLADE SURGICAL #15 STAINLESS STEEL (1) BLADE SURGICAL #11 STAINLESS STEEL (1) GOWN IMPERV. EXTRA REINFORCED XLG (1) GOWN LGE STANDARD SMS VELCRO NECK (1) IRRIGATION SUCTION TROMPET DUAL SPIKE (10) GAUZE SPONGE 4" X 4" 16PLY XRD (2) UTILITY BOWL 16oz (2) STERI STRIP CLOSURE W' X 4" (1) ACTIFOG W/
Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.
- 2014-08-14CPSCArctic Cat Inc., of Thief River Falls, Minn.Snowmobiles Recalled by Arctic Cat Due to Fuel Leak and Fire Hazard (Recall Alert)
Fuel can leak from the fuel line assembly, posing a fire hazard.
- 2014-08-13FDA-DeviceStryker Instruments Div. of Stryker CorporationClass IISonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.
The firm received complaints regarding insufficient irrigation to the tip of the Sonopet system. Lack of irrigation can potentially lead to excessive heat at the tip.
- 2014-07-09FDA-FoodOlde Thompson, Inc.Class IKirkland Signature Coarse Ground Malabar Pepper, 12.7 oz Plastic Jars, UPC 096619164998. Packaging includes a PET bottle. The lid is made of Polypropylene and contains a tinplate insert and a Polypropylene five-hole cap. The label on the jar is a rectangular label (front and back) information is superimposed over an antique map in various shades of brown.
Olde Thompson is recalling Kirkland Signature Coarse Ground Malabar Black Pepper because it may be contaminated with Salmonella.
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