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. 2,789 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,789 in last 12 months

Showing 1178111800 of 51,768 recalls

Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono biplane- Model No. 11327600 Artis icono floor- Model No....

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model Recalled by Siemens...

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis pheno- Model No. 10849000 Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· Hologic, Inc

Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...

The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...

The Issue: Firm noted an increase in customer reports of leaks.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2022· Technomed Europe

Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...

The Issue: Burns of varying degrees can occur to patients with electrodes left in while...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2022· Akorn, Inc

Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc Due to...

The Issue: Identification of an unknown impurity at the 12-month stability point....

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 8, 2022· GS Biomark LLC

Recalled Item: CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200...

The Issue: Distribution of COVID Test Kits without FDA Approval, Clearance or...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2022· LNK International, Inc.

Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets Recalled by LNK...

The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as...

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2022· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2022· That's it. Nutrition, LCC

Recalled Item: That's It. Dark Chocolate Raisin Truffles Net WT. 3.5 oz Recalled by That's...

The Issue: CFIA testing of the products revealed casein and whey which caused...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2022· That's it. Nutrition, LCC

Recalled Item: That's It. Dark Chocolate Fig with Sea Salt Truffles Net WT. 3.5 oz Recalled...

The Issue: CFIA testing of the products revealed casein and whey which caused...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2022· That's it. Nutrition, LCC

Recalled Item: That's It. Dark Chocolate Fig Truffles Net WT. 3.5 oz Recalled by That's it....

The Issue: CFIA testing of the products revealed casein and whey which caused...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2022· That's it. Nutrition, LCC

Recalled Item: That's It. Dark Chocolate Banana Truffles Net WT. 3.5 oz Recalled by That's...

The Issue: CFIA testing of the products revealed casein and whey which caused...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2022· That's it. Nutrition, LCC

Recalled Item: That's It. Dark Chocolate Date Truffles Net WT. 3.5 oz Recalled by That's...

The Issue: CFIA testing of the products revealed casein and whey which caused...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2022· Eclectic Institute Inc

Recalled Item: Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement Recalled by...

The Issue: Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 3, 2022· Merit Medical Systems, Inc.

Recalled Item: CorVocet Biopsy System/Catalog Code: CORA1610/B Recalled by Merit Medical...

The Issue: Biopsy Systems have components that are misaligned due to an issue with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Merit Medical Systems, Inc.

Recalled Item: CorVocet Biopsy System Recalled by Merit Medical Systems, Inc. Due to Biopsy...

The Issue: Biopsy Systems have components that are misaligned due to an issue with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Wright Medical Technology, Inc.

Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...

The Issue: The outer label does not match the device inside the package. The affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Wright Medical Technology, Inc.

Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...

The Issue: The outer label does not match the device inside the package. The affected...

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

Class II — Potential Health HazardOngoing