Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 3,047 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,047 in last 12 months

Showing 49414960 of 30,923 recalls

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· 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 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 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...

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 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915...

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 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...

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 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 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· Alphatec Spine, Inc.

Recalled Item: IdentiTi ALIF Standalone Interbody System: Part Number/Description...

The Issue: Due to reports of intraoperative graft bolt implantation breakages.

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

Class II — Potential Health HazardOngoing
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· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with:...

The Issue: Due to a trend in false positive Candida tropicalis results on blood culture...

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· Thommen Medical AG

Recalled Item: impression coping Recalled by Thommen Medical AG Due to The depth of the...

The Issue: The depth of the internal canal was not manufactured according to...

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