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. 2,840 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,840 in last 12 months

Showing 31413160 of 51,768 recalls

Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid MR IMRIS Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Operating table column TS7500 MOBIUS Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Progressa Bed Surfaces Recalled by Baxter Healthcare Corporation Due to The...

The Issue: The air bladders inside the mattress may move out of position when the head...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid (FC) Recalled by Baxter Healthcare Corporation...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid Plus (SC) Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Floor mounting column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Floor mounting column TS 7500 U Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Mobile column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
DrugFebruary 24, 2025· Denison Pharmaceuticals, LLC

Recalled Item: Zapzyt Recalled by Denison Pharmaceuticals, LLC Due to Chemical...

The Issue: Chemical Contamination: Presence of benzene.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
FoodFebruary 23, 2025· Prep'd CDA LLC

Recalled Item: Chocolate Peanut Butter Protein Balls. Product has expected life of Recalled...

The Issue: Undeclared soy lecithin and undeclared color additives Blue 1 Lake, Yellow...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 21, 2025· Shearer's Foods, LLC

Recalled Item: 1.) Market Pantry Soup & Oyster Crackers Recalled by Shearer's Foods, LLC...

The Issue: Potential foreign material (stainless steel wire)

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2025· One Source Nutrition, Inc,

Recalled Item: Vitality Recalled by One Source Nutrition, Inc, Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 20, 2025· Central Admixture Pharmacy Services, Inc.

Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2025· BD SWITZERLAND SARL

Recalled Item: BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to...

The Issue: Due to specific lots of luer-lok devices were shipped to the U.S. market...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2025· Orthofix U.S. LLC

Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...

The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2025· Microbiologics Inc

Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...

The Issue: The RSV target may give a late Ct value and could potentially not pass QC.

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

Class II — Potential Health HazardOngoing