Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,530 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,530 in last 12 months

Showing 46814700 of 27,254 recalls

Medical DeviceJanuary 29, 2024· SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION

Recalled Item: Shimadzu Recalled by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Due to...

The Issue: Due to capacitor manufacturing issue, their is a potential that Flat Panel...

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 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· 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· In2Bones, SAS

Recalled Item: I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm 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 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 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 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: 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: 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: 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