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. 2,653 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,653 in last 12 months

Showing 2472124740 of 51,768 recalls

DrugNovember 15, 2018· Fresenius Kabi USA, LLC

Recalled Item: SODIUM CHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 15, 2018· Fresenius Kabi USA, LLC

Recalled Item: SODIUM CHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2018· 4Patriots, LLC

Recalled Item: 4Patriots Chicken a la King CONTAINS: Wheat Recalled by 4Patriots, LLC Due...

The Issue: Milk not declared on product label.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 15, 2018· Prollenium Medical Technologies Inc.

Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...

The Issue: Labeling error. The product is labeled with an 18 month expiration date,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2018· GE Healthcare, LLC

Recalled Item: Various GE Magnetic Resonance System on-site software version Product Usage:...

The Issue: Possible incorrect software version loaded.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2018· Covidien LLC

Recalled Item: Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2018· Covidien LLC

Recalled Item: Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2018· Covidien LLC

Recalled Item: Covidien Emprint Short Percutaneous Antenna with Thermosphere Technology...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
DrugNovember 14, 2018· Ascend Laboratories LLC

Recalled Item: Quetiapine Tablets USP 400 mg Recalled by Ascend Laboratories LLC Due to...

The Issue: Presence of Foreign Substance; metal shard found in tablet

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2018· Arrow International Inc

Recalled Item: Arrow CVC 2 Lumen Recalled by Arrow International Inc Due to The lidstock...

The Issue: The lidstock states the incorrect priming volume and flow rates.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2018· Diagnostica Stago, Inc.

Recalled Item: Staclot LA 20 () The Staclot¿ LA and Staclot¿ Recalled by Diagnostica Stago,...

The Issue: There have been reports of shortened (T1-T2) results, where some instances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2018· Diagnostica Stago, Inc.

Recalled Item: Staclot¿ LA () The Staclot¿ LA and Staclot¿ LA Recalled by Diagnostica...

The Issue: There have been reports of shortened (T1-T2) results, where some instances...

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

Class II — Potential Health HazardOngoing
FoodNovember 13, 2018· Smartypants Vitamins

Recalled Item: Smartypants Kids Complete Recalled by Smartypants Vitamins Due to Foreign...

The Issue: Consumer complaints of finding foreign objects in bottles of gummy vitamins.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 13, 2018· Stryker Communications

Recalled Item: EDS Light Suspension Recalled by Stryker Communications Due to There is a...

The Issue: There is a potential the joint in the suspension of the device is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2018· RVO 2.0, INC

Recalled Item: Raindrop Near Vision Inlay Recalled by RVO 2.0, INC Due to During a post...

The Issue: During a post approval study the firm found there was an increased risk of...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 13, 2018· bioMerieux, Inc.

Recalled Item: VITEK¿ 2 Systems Software Version 9.01 Update Kit. Recalled by bioMerieux,...

The Issue: The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to Isocenter shifts...

The Issue: Isocenter shifts when using dose tracking in RayStation 3.5, RayStation 4.0,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2018· Bracco Injeneering S.A.

Recalled Item: Empower FastLoad CT Syringe Pack -sterile disposable syringe kit for...

The Issue: Insufficient seal on the sterile barrier of the device, compromising the...

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

Class II — Potential Health HazardOngoing
DrugNovember 9, 2018· Ecolab Inc

Recalled Item: Equi-Soft Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...

The Issue: Labeling: Label mix-up - the label on the product may not match the formula...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2018· Ecolab Inc

Recalled Item: Medi-Stat Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...

The Issue: Labeling: Label mix-up - the label on the product may not match the formula...

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

Class II — Potential Health HazardOngoing
Refund