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. 2,612 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,612 in last 12 months

Showing 3212132140 of 51,768 recalls

Medical DeviceFebruary 28, 2017· Stryker Communications

Recalled Item: The Stryker Visum¿ LED Surgical Lighting system is intended to Recalled by...

The Issue: The potential hazard that can arise for the combination of the missing...

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

Class II — Potential Health HazardOngoing
FoodFebruary 27, 2017· Versa Marketing

Recalled Item: Fusia Asian Aspirations Szechuan Stir Fry Recalled by Versa Marketing Due to...

The Issue: Product was tested and found positive for Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2017· LIEBEL-FLARSHEIM COMPANY LLC

Recalled Item: Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim...

The Issue: Software issue. The difference between the display and dosimeter readings In...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· LIEBEL-FLARSHEIM COMPANY LLC

Recalled Item: Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim...

The Issue: Software issue. The difference between the display and dosimeter readings In...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Zimmer Biomet, Inc.

Recalled Item: MEDTECH ROSA Spine 1.0.2 The device is intended for the Recalled by Zimmer...

The Issue: Unapproved change made by the supplier.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Welch Allyn Inc

Recalled Item: Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400 Recalled by Welch...

The Issue: A defective electrical component in the battery charging circuit in two lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Zimmer Biomet, Inc.

Recalled Item: MEDTECH ROSA Brain 3.0 The device is intended for the Recalled by Zimmer...

The Issue: Unapproved change made by the supplier.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q and Q.Zen fluoroscopic x-ray system Recalled by Siemens Medical...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee and Zeego fluoroscopic x-ray system Recalled by Siemens Medical...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis fluoroscopic x-ray system Recalled by Siemens Medical Solutions...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
DrugFebruary 24, 2017· Citron Pharma Llc

Recalled Item: Penicillin V Potassium Tablets Recalled by Citron Pharma Llc Due to Presence...

The Issue: Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 24, 2017· Manzana Products Co., Inc.

Recalled Item: Trader Joe's First Crush Unsweetened Gravenstein Apple Sauce Recalled by...

The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2017· Manzana Products Co., Inc.

Recalled Item: Trader Joe's Organic Unsweetened Apple Sauce Recalled by Manzana Products...

The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2017· Manzana Products Co., Inc.

Recalled Item: Trader Joe's All Natural Unsweetened Apple Sauce Recalled by Manzana...

The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2017· Trader Joes Company

Recalled Item: Trader Joes Imported English Authentic Lemon Curd Recalled by Trader Joes...

The Issue: Trader Joe's Co. is recalling the Lemon Curd because it contains undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2017· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...

The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT model number 882482 BrightView and BrightView X are Recalled...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X 3/4 model number 882479 BrightView and BrightView X Recalled by...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X 3/8 model number 882478 BrightView and BrightView X Recalled by...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT model number 882480 BrightView and BrightView X are...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing