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. 2,433 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,433 in last 12 months

Showing 4866148680 of 51,768 recalls

FoodMarch 1, 2013· Bay Valley Foods LLC/ TreeHouse Foods, Inc

Recalled Item: 55613210946 Western Family Recalled by Bay Valley Foods LLC/ TreeHouse...

The Issue: Bay Valley Foods is voluntarily recalling approximately 430,227 cases of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bay Valley Foods LLC/ TreeHouse Foods, Inc

Recalled Item: 556132100582 Meijer Recalled by Bay Valley Foods LLC/ TreeHouse Foods, Inc...

The Issue: Bay Valley Foods is voluntarily recalling approximately 430,227 cases of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bay Valley Foods LLC/ TreeHouse Foods, Inc

Recalled Item: 55613205218 Pasta on the Side Recalled by Bay Valley Foods LLC/ TreeHouse...

The Issue: Bay Valley Foods is voluntarily recalling approximately 430,227 cases of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 1, 2013· American Medical Systems, Inc.

Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...

The Issue: American Medical Systems, Inc. is initiating a recall on two components of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· American Medical Systems, Inc.

Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...

The Issue: American Medical Systems, Inc. is initiating a recall on two components of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· B. Braun Medical, Inc.

Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...

The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...

The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse...

The Issue: An internal protective fuse can be unintentionally activated while the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mammomat Inspiration - full-field digital mammography Product Usage:...

The Issue: Firm became aware of an unintended behavior when using the Mammomat...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2013· Allen Medical Systems, Inc.

Recalled Item: Allen Traction Boot Recalled by Allen Medical Systems, Inc. Due to Some...

The Issue: Some units may have been assembled incorrectly which could result in the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: FIBRICOR (fenofibric acid) Tablets Recalled by Mutual Pharmaceutical...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Labeling Wrong Barcode; It may display wrong product code 0.9% Sodium...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2013· Koda Farms Inc

Recalled Item: Mochiko Blue Star Sweet Rice Flour Recalled by Koda Farms Inc Due to Koda...

The Issue: Koda Farms received a report from a customer that a hard yellow material was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2013· Hospira Inc.

Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...

The Issue: The infusion pump has a clear plastic door that, due to its design, allows...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Hospira Inc.

Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...

The Issue: The infusion pump has a clear plastic door that, due to its design, allows...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...

The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...

The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 with Venous blood parameter...

The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...

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

Class II — Potential Health HazardOngoing