Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,439 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,439 in last 12 months

Showing 4696146980 of 51,768 recalls

FoodJuly 3, 2013· Crave Brothers Farmstead Cheese, LLC

Recalled Item: Crave Brothers Farmstead Classics Les Freres Semi-Soft French Style Cheese...

The Issue: Crave Brothers Farmstead Cheese Company is recalling 3 specialty cheese...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 3, 2013· Crave Brothers Farmstead Cheese, LLC

Recalled Item: Crave Brothers Farmstead Classics Petit Frere Soft Ripened Cheese Recalled...

The Issue: Crave Brothers Farmstead Cheese Company is recalling 3 specialty cheese...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 3, 2013· Crave Brothers Farmstead Cheese, LLC

Recalled Item: Crave Brothers Farmstead Classics Petit Frere with Truffles Cheese Recalled...

The Issue: Crave Brothers Farmstead Cheese Company is recalling 3 specialty cheese...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 3, 2013· NOW Foods

Recalled Item: White plastic bottle with blue cap containing 90 capsules Recalled by NOW...

The Issue: It has been determined that this product contains an undeclared ingredient,...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Reservoirs Recalled by Medtronic MiniMed Due to...

The Issue: Medtronic is recalling certain lots of Medtronic MiniMed Paradigm Reservoirs...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 2, 2013· Core Pharma Llc

Recalled Item: Pyridostigmine Bromide Tablets 60 mg Recalled by Core Pharma Llc Due to...

The Issue: Failed Stability Specifications: Pyridostigmine Bromide tablets, is being...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL Recalled by...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER Recalled by Ecolab Inc...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL Recalled by Ecolab...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER Recalled by Ecolab Inc Due...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL Recalled by Ecolab...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL Recalled by...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System Radiation treatment planning Recalled by Elekta, Inc. Due...

The Issue: Upgrade installation script is designed to overwrite the same pouch files in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp...

The Issue: Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 1, 2013· Fresenius Kabi USA, LLC

Recalled Item: Benztropine Mesylate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of particulate matter: characterized as thin colorless flakes that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 1, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL...

The Issue: Siemens initiated a recall due to confirmed complaints of low patient sample...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Iradimed Corporation

Recalled Item: MRidium 1145 Dose Reduction System (DERS) drug library kit. (This Recalled...

The Issue: The Dose Error Reduction System (DERS) can indicate an incorrect recommended...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RemB Electric Universal Driver For use with the Recalled by Stryker...

The Issue: The safety margin values detailed in the Engineering Design were entered...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...

The Issue: The safety margin values detailed in the Engineering Design were entered...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...

The Issue: The safety margin values detailed in the Engineering Design were entered...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing