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. 2,728 recalls have been distributed to Washington in the last 12 months.
Showing 18001–18020 of 51,768 recalls
Recalled Item: Blood Monitoring Unit (BMU 40) Recalled by Maquet Cardiovascular Us Sales,...
The Issue: The Printed Circuit Board Assembly (PCBA) are not in compliance with the IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRADER JOE S TRADER POTATO TOTS is frozen potatoes Recalled by J .R. Simplot...
The Issue: Product was recalled due to small pieces of plastic or rubber material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BladderScan Prime Plus Probe - Product Usage: intended Recalled by Verathon,...
The Issue: Due to a change in handle material and process, probe handle may crack.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluocinonide Ointment USP 0.05% Recalled by Teligent Pharma, Inc. Due to...
The Issue: Failed Impurities/Degradation - Out-of-specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SKIPPY Super Chunk Peanut Butter 16.3oz packaged in Recalled by Hormel Foods...
The Issue: Aflatoxin level slightly above actionable limit
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VNS Therapy¿ AspireSR¿ Generator Recalled by LivaNova USA Inc Due to Due to...
The Issue: Due to an extra digit being inadvertently added to the serial number of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB PowerCel 170 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB PowerCel 230 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Happy Ducts Compress Recalled by Wishgarden Herbs, Incorporated Due to...
The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Goldenseal POWDER Recalled by Wishgarden Herbs, Incorporated Due to...
The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cord Care POWDER Recalled by Wishgarden Herbs, Incorporated Due to Microbial...
The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NYSTATIN ORAL SUSPENSION Recalled by VistaPharm, Inc. Due to Failed...
The Issue: Failed Impurties/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Newly Weds Foods G44384 Cinnamon Snack Seasoning X1 Recalled by Newly Weds...
The Issue: potentially contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Newly Weds Foods S13823 Berbere Seasoning Blend X1 Recalled by Newly Weds...
The Issue: potentially contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Osteosynthesis Compression Staple EasyClip Recalled by Stryker GmbH Due to...
The Issue: The device has the potential to release nickel above the acceptable margin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIDEL Sofia SARS Antigen FIA IVD Recalled by Quidel Corporation Due to Due...
The Issue: Due to false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien MONOJECT Standard Hypodermic Needle Recalled by Cardinal Health...
The Issue: Potential for the needle to detach from the cartridge after the bottom of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Platform Fracture Stem Recalled by Exactech, Inc. Due to The device...
The Issue: The device may be incorrectly laser marked as a right stem, when it should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Platform Fracture Stem Recalled by Exactech, Inc. Due to The device...
The Issue: The device may be incorrectly laser marked as a right stem, when it should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.