Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,646 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,646 in last 12 months

Showing 1180111820 of 29,201 recalls

Medical DeviceMay 22, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as Recalled...

The Issue: Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2020· Tosoh Bioscience Inc

Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to The Substrate...

The Issue: The Substrate Monitoring System in the AIA-900 Analyzer did not detect an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2020· Vitalconnect Inc.

Recalled Item: VistaSolution Recalled by Vitalconnect Inc. Due to A healthcare provider...

The Issue: A healthcare provider (HCP) noticed a patient had a lowered historic SpO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System - Software Versions 3.3.3 and Recalled by...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Software Versions 3.5.1 and below Recalled...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Software Versions 3.3.3 and below Product...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System - Product Code: 6802914 Unique Recalled...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Leica Microsystems, Inc.

Recalled Item: Leica ARveo and M530 OH6 microscope systems. Recalled by Leica Microsystems,...

The Issue: Possible unintended interruption of surgical procedures due to equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2020· ROi CPS LLC

Recalled Item: Isolation Droplet Bundle Kit Recalled by ROi CPS LLC Due to Roi CPS, LLC has...

The Issue: Roi CPS, LLC has become aware of a labeling error that affects select custom...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2020· ROi CPS LLC

Recalled Item: Respirator Crash Cart Kit Recalled by ROi CPS LLC Due to Roi CPS, LLC has...

The Issue: Roi CPS, LLC has become aware of a labeling error that affects select custom...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2020· Philips North America, LLC

Recalled Item: Philips SureSigns VM1SpO2 Recalled by Philips North America, LLC Due to...

The Issue: Philips has identified a Philips SureSigns VM1 monitor in the possession of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· Carefusion 2200 Inc

Recalled Item: Mueller Knife Handle Recalled by Carefusion 2200 Inc Due to Becton Dickinson...

The Issue: Becton Dickinson and Company, is conducting a voluntary recall on the V....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Service Pack 2 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8A Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 5 Service Pack 3 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Service Pack 3 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9A Recalled by RAYSEARCH LABORATORIES AB Due to Software error...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Recalled by RAYSEARCH LABORATORIES AB Due to Software error...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing