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.
- 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.
- 2018-09-05FDA-DeviceStryker Leibinger GmbH & Co. KGClass IIQUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01531S, 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 IIQUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01530S, 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 IIQUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01521S The Stryker QuickFlap Sterile Procedure Pack is intended for reconstruction, stabilization and/or rigid fixation of non-load bearing bony areas subsequent to craniotomy, craniectomy and cranial fractures in adults and adolescents (age 12 and higher).
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 IIQUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01520S The Stryker QuickFlap Sterile Procedure Pack is intended for reconstruction, stabilization and/or rigid fixation of non-load bearing bony areas subsequent to craniotomy, craniectomy and cranial fractures in adults and adolescents (age 12 and higher).
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
- 2018-09-05FDA-FoodThe Coca-Cola CompanyClass IIConsumer Packaging (PET bottle): Minute Maid TROPICAL BLEND Flavored Juice Beverage 12 FL OZ (355mL), JAN0719NPA, UPC: 0 25000 06229 2. Master Case: packaged 24/12 fl.oz., GTIN number 00025000062414 (no UPC)
Foreign matter believed to be glass observed in retain samples of product.
- 2018-08-29CPSCBSN SPORTS LLC, of Farmers Branch, TexasBSN SPORTS Recalls Rubber Critter Toys Due to Violation of Federal Lead Paint Ban (Recall Alert)
The orange and yellow surface paint on the rubber critter toys contains levels of lead that exceed the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- 2018-08-15FDA-DeviceThink Surgical, Inc.Class IIThink Surgical Cutter, Flat, ¿6.2mm x 144mm. For use only with the TCAT Computer-Assisted Tool. Part Number 106428 The cutter is used to prepare the bone for the (TKA) Total Knee Arthroplasty.
There is a potential for the cutter head to detach from the cutter shaft.
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IICT Goldseal BrightSpeed 16 PWR TIO 2 YR
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IIOptima CT 540
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IIOptima CT 520
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IIRevolution EVO 3.6, labeled as a. HVY WAUK; b. LONG HINO; c. LONG WAUK; d. MID BJG; e. MID WAUK.
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IICT Goldseal Optima CT 600
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IIRevolution CT 160 1.5D STD WAUK
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IIDiscovery RT labeled as: a. MID BJG; b. HVY BJG
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IIDiscovery MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IIDiscovery MI Digital Ready
DIGITAL ReadyCT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08FDA-DeviceGE Healthcare, LLCClass IIDiscovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- 2018-08-08CPSCPolaris Industries Inc., of Medina, Minn.Bobcat Company Recalls Utility Vehicles Due To Burn and Fire Hazards (Recall Alert)
The utility vehicle's exhaust header pipe can crack, posing burn and fire hazards.
- 2018-08-02CPSCArctic Cat Inc., of Thief River Falls, Minn., a subsidiary of Textron Specialized Vehicles, of Augusta, Ga.Arctic Cat Snowmobiles Recalled by Textron Specialized Vehicles Due to Injury Hazard (Recall Alert)
The handgrip can break, posing an injury hazard to the rider.
- 2018-08-01FDA-DeviceLeica Microsystems, Inc.Class IILeica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419, 10448420, 10448485, 10448486 Product Usage: Intended use of this device is an optical instrument for magnifying and illuminating specimens. It can be applied for observation and documentation and for human and veterinary medical treatment. Not for use in Eye Operations.
Possible failure of screws which hold the gas spring fixation bracket in place. Due to this failure, the gas spring, which is fixed to the upper part of the parallelogram, cannot hold up the weight of the optics carrier.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve, Trumpet Valve, No Probe, Double Spike, Ref ASU1221, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
The suction valve may not close properly which could cause continuous suction.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve, Trumpet Valve, No Probe, Single Spike, Ref ASU1220, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
The suction valve may not close properly which could cause continuous suction.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Double Spike, Ref ASU1211, packaged 1/box, 12 boxes/case, single use, RX, Sterile. Manufactured For Cardinal Health, Waukegan, IL.
The suction valve may not close properly which could cause continuous suction.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Single Spike, Ref ASU1210, packaged 1/box, 12 boxes/case, single use, RX, Sterile. .
The suction valve may not close properly which could cause continuous suction.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Double Spike, Ref ASU1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
The suction valve may not close properly which could cause continuous suction.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Single Spike, Ref ASU1200, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
The suction valve may not close properly which could cause continuous suction.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Double Spike and no Probe, Ref ASC1221, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
The suction valve may not close properly which could cause continuous suction.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Single Spike and no Probe, Ref ASC1220, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
The suction valve may not close properly which could cause continuous suction.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Double Spike, Ref ASC1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
The suction valve may not close properly which could cause continuous suction.
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