Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,581 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,581 in last 12 months

Showing 66616680 of 27,833 recalls

Medical DeviceMarch 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System - . For use in Recalled by Ortho-Clinical...

The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Input Output Module (IOM) FLX-201-Laboratory Automation system Brand names...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: PVT Interface Module (PVT)-Laboratory Automation system Brand names of the...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Inpeco S.A.

Recalled Item: Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of...

The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2023· Alcon Research, LLC

Recalled Item: Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Recalled by Alcon...

The Issue: Sterility; Steril surgical procedure packs contain incomplete seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2023· DeVilbiss Healthcare LLC

Recalled Item: DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR Recalled by DeVilbiss...

The Issue: The instruction manual is being replaced with an updated version that is in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody...

The Issue: Incorrect Number of Calibrator Levels (2) Set for the VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2023· Philips North America Llc

Recalled Item: Philips DigitalDiagnost C50 -intended for use in generating radiographic...

The Issue: If the PM for the telescopic carriage is not performed annually as defined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C50 1.1-intended for use in generating radiographic images...

The Issue: If the PM for the telescopic carriage is not performed annually as defined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· Medacta Usa Inc

Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H10 Recalled by Medacta Usa Inc Due to...

The Issue: There is a potential for breakage of the small screw used to affix the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· Radiometer Medical ApS

Recalled Item: AQURE Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 Recalled by Radiometer...

The Issue: Due to potential software issue that may result in patient mix-up information.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· Medacta Usa Inc

Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H14 Recalled by Medacta Usa Inc Due to...

The Issue: There is a potential for breakage of the small screw used to affix the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems Recalled by...

The Issue: Due to manufacturing issue, Gastrointestinal (GI) Panel may result in false...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· Medacta Usa Inc

Recalled Item: MectaLIF ANTERIOR - Antibackout Lag Cover Recalled by Medacta Usa Inc Due to...

The Issue: There is a potential for breakage of the small screw used to affix the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· Medacta Usa Inc

Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H18 Recalled by Medacta Usa Inc Due to...

The Issue: There is a potential for breakage of the small screw used to affix the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· Medacta Usa Inc

Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H12 Recalled by Medacta Usa Inc Due to...

The Issue: There is a potential for breakage of the small screw used to affix the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· Medacta Usa Inc

Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H16 Recalled by Medacta Usa Inc Due to...

The Issue: There is a potential for breakage of the small screw used to affix the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2023· NeuroLogica Corporation

Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...

The Issue: Issue related to the operation of the arm latch within the column that...

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

Class II — Potential Health HazardOngoing