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. 1,012 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,012 in last 12 months

Showing 36021–36040 of 51,768 recalls

FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 1/4" Frozen WHITE Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: IQF 1/4" White Onion Dice is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 3/8" Un-Blanched Yellow Onion Dice Recalled by Oregon Potato Company Due...

The Issue: IQF 3/8" Un-Blanched, Frozen, Yellow Onion Dice is voluntarily recalled...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 3/4" Yellow Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: IQF 3/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 3/8" Yellow Onion Strip Recalled by Oregon Potato Company Due to...

The Issue: IQF 3/8" Frozen Yellow Onion Strip and IQF 3/8" Yellow ORGANIC Onion Strip...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: 3/8" White Onion Dice- FRESH Recalled by Oregon Potato Company Due to...

The Issue: 3/8" White Onion Dice- FRESH is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 1/4" Yellow Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: IQF 1/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: 705000 IQF 3/8" Dice Yellow Onion Recalled by Oregon Potato Company Due to...

The Issue: 3/8" Frozen Yellow Onion Dice was voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: 3/8" White Onion Strip-FRESH Recalled by Oregon Potato Company Due to...

The Issue: 3/8" White Onion Strip-FRESH was voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 1/4 x 1/4 Yellow Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: 1/4 x 1/4 Frozen Yellow Onion Dice was voluntarily recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 5, 2016· Empirical Laboratories, Incorporated

Recalled Item: Liposomal Magnesium Nutritional Supplement. 6 FL. OZ (180 ml) The Recalled...

The Issue: Empirical Labs is recalling Liposomal Magnesium because of the potential for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 5, 2016· Ceg Enterprises Llc

Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...

The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...

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

Class II — Potential Health HazardOngoing
DrugApril 5, 2016· Fresenius Kabi USA, LLC

Recalled Item: Cisatracurium Besylate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Incorrect/ Undeclared Excipient: Firm is recalling product due to an...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 4, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril & Hydrochlorothiazide Tables Recalled by Lupin Pharmaceuticals...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. Product Usage: Merge Hemo is a hemodynamic Recalled by...

The Issue: In some instances, the system will lock tabs within a study, even when a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive when used with RadSuite. The firm name Recalled...

The Issue: The software produced a number of "do not route" exceptions, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare....

The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...

The Issue: When taking measurements from images on the Cardio workstation or from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station and Merge Eye Care PACS. Recalled by Merge Healthcare,...

The Issue: During an antivirus program scan of the Eye Station or Eye Care PACS, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. The firm name on the labeling is Merge Healthcare...

The Issue: Use of the software may show an incorrect value to the user when viewing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Mesa Laboratories Inc

Recalled Item: ProSpore 4 mL Ampoule Biological indicator for steam sterilization Recalled...

The Issue: Product resistance has fallen outside of label claim within expiry.

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

Class II — Potential Health HazardOngoing