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. 2,820 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,820 in last 12 months

Showing 47814800 of 29,208 recalls

Medical DeviceJanuary 26, 2024· BioFire Diagnostics, LLC

Recalled Item: FilmArray Gastrointestinal (GI) Panel RFIT-ASY-0116 (30 test kit)...

The Issue: Due to potential signals of increased false positive Norovirus results when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 3600 Immunodiagnostic System Catalog Nos. 6802783 (regular) and...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· In2Bones, SAS

Recalled Item: I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm Recalled by In2Bones,...

The Issue: This Field Action is being conducted following the identification of a batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 3400 Chemistry System Recalled by Ortho-Clinical Diagnostics, Inc....

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...

The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2024· Voco GmbH

Recalled Item: Ionolux Recalled by Voco GmbH Due to Due to an error in the manufacturing...

The Issue: Due to an error in the manufacturing process, it is possible that an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2024· Voco GmbH

Recalled Item: IonoStar Plus Recalled by Voco GmbH Due to Due to an error in the...

The Issue: Due to an error in the manufacturing process, it is possible that an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2024· Raye's Inc.

Recalled Item: SW Bari Lift & Transfer Recalled by Raye's Inc. Due to Retrospective...

The Issue: Retrospective engineering analysis against current ISO standards for hoists...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: RIA Tube Assembly Recalled by Synthes (USA) Products LLC Due to Products not...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: Opal Recalled by Synthes (USA) Products LLC Due to Products not sterilized,...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: RAPIDSORB IPS Battery Pack Recalled by Synthes (USA) Products LLC Due to...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX Recalled by Synthes...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: TFNA Femoral Nail 9mm Recalled by Synthes (USA) Products LLC Due to Products...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: 1.5MM Drill Bit/QC/85MM Sterile-surgical Recalled by Synthes (USA) Products...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: VA-LCP Clavicle Plate 2.7 Recalled by Synthes (USA) Products LLC Due to...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: 2.5MM DRILL BIT/QC/GOLD/110MM STERILE-surgical Recalled by Synthes (USA)...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: TFNA Femoral Nail 11mm Recalled by Synthes (USA) Products LLC Due to...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing