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. 2,602 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,602 in last 12 months

Showing 3628136300 of 51,768 recalls

DrugMarch 15, 2016· Hospira Inc.

Recalled Item: Quelicin (Succinylcholine Chloride) Injection Recalled by Hospira Inc. Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot...

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

Class III — Low RiskOngoing
Refund
FoodMarch 15, 2016· Nuwati Herbals Inc

Recalled Item: Nuwati Herbals SeeLessO'Me Diet and Weight Management Tea packaged in...

The Issue: Product contains undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Foot Section for Semi & Full Electric Beds Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed with mattress and rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed w/o mattress & rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Junction Boxes Recalled by Invacare Corporation Due to The firm recently...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Ventlab LLC

Recalled Item: STAT-Check Resuscitation Bag Manual Emergency Resuscitation Bag with Carbon...

The Issue: Stat-check CO2 indicators are non-functional. The indicator is yellow when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF used with an Recalled...

The Issue: New reprocessing instructions for the Olympus TJF-160/VF duodenoscopes,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The vacuum suction...

The Issue: The vacuum suction tubing could be kinked within the machine resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 for Proton Radiation Therapy Recalled by Mevion Medical Systems,...

The Issue: Possibility of Gantry Motion with Aperture or Compensator only partially...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2016· Impax Laboratories, Inc.

Recalled Item: Dextroamphetamine Sulfate Tablets USP Recalled by Impax Laboratories, Inc....

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Impax Laboratories, Inc.

Recalled Item: Dextroamphetamine Sulfate Tablets USP Recalled by Impax Laboratories, Inc....

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 4 (Papaverine 18 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 0 (PGE 20 mcg/mL) Injection Recalled by Meditech Laboratories, Inc...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 9 (Papaverine 0.9 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 3 (Papaverine 20 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 1 (Papaverine 1.8 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Superpotent Drug: one ingredient was found to be above assay specification.

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

Class II — Potential Health HazardOngoing
Refund