Pet food and pet product recalls
1058 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.
- 2018-08-08FDA-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.
- 2018-07-25FDA-DeviceCardinal Health 200, LLCClass IIHydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Single Spike, Ref ASC1200, 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, Cassette Trumpet Valve with Bariatric Probe, Double Spike, Ref ABP1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
The suction valve may not close properly which could cause continuous suction.
- 2018-07-18FDA-DevicebioMerieux, Inc.Class IIBioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS (QCV) is an automated test for use on the VIDAS¿ system to detect abnormal operation of the VIDAS and mini VIDAS instrument pipette mechanisms and optical systems. Specifically the mini VIDAS system is an immunodiagnostic system intended to be used by trained and qualified laboratory professionals, for In vitro Diagnostic (IVD) purpose, veterinary and industrial applications. Th
Increase of events affecting performance regarding pump clogging and displacement of the color-coded SPR label (DOT). These performance issues could contribute to erroneous results for any assay performed on the VIDAS¿ and mini VIDAS¿ system due to a decrease of pipetted volume.
- 2018-07-18FDA-DevicebioMerieux, Inc.Class IIBioMerieux mini VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS (QCV) is an automated test for use on the VIDAS¿ system to detect abnormal operation of the VIDAS and mini VIDAS instrument pipette mechanisms and optical systems. Specifically the mini VIDAS system is an immunodiagnostic system intended to be used by trained and qualified laboratory professionals, for In vitro Diagnostic (IVD) purpose, veterinary and industrial application
Increase of events affecting performance regarding pump clogging and displacement of the color-coded SPR label (DOT). These performance issues could contribute to erroneous results for any assay performed on the VIDAS¿ and mini VIDAS¿ system due to a decrease of pipetted volume.
- 2018-07-18FDA-FoodTalking Rain Beverage Co IncClass IISparkling ICE Cherry Limeade Naturally Flavored Sparking Water, packaged in a PET bottles with a plastic cap, Net Wt. 17 ounces (502.8 ml). UPC code on bottle: 0 16571 95084 2. UPC on Single Pack Wrapper (1 flavor/12 bottles): 016571953126 UPC on Single Pack Wrapper (1 flavor/24 bottles): NONE ****************************************************************************************** Sparkling ICE Cherry Limeade is also assembled and sold in Variety Packs with other flavors (those other
Sparkling ICE Cherry Limeade, 17 oz. bottles, is recalled after the firm received a small number of customer complaints that reported an off-taste and off-odor of the product.
- 2018-07-12CPSCAllura Imports, of New YorkAllura Recalls Children's Sleepwear Due to Violation of Federal Flammability Standard
The children's pajamas fail to meet the flammability standard for children's sleepwear, posing a risk of burn injuries to children.
- 2018-07-11FDA-DeviceHowmedica Osteonics Corp.Class IILFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-236
The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011.
- 2018-06-27FDA-DeviceCyberonics, IncClass IIVNS Therapy Programmer, Model 3000, v1.0 System
Certain Model 3000 programming events can result in miscalculation of parameters stored in the Models 103, 104, 105, and 106 generators. During these programming events, the miscalculations can lead to: " Delivery of more stimulation than intended, resulting in painful stimulation or other common side effects (Model 106 only); " No stimulation in the case of device disablement (Burst Watchdog Timeout), resulting in no therapy to the patient (Model 106 only); " Delivery of less stimulation than intended, resulting in therapeutic settings not being achieved within device specification (Models 103, 104, 105, or 106); and/or " Delays or absence of the 75% and 50% battery life indicators displayed by the programming software (Models 103, 104, 105, or 106).
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