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. 2,604 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,604 in last 12 months

Showing 1630116320 of 29,201 recalls

Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: 1) Vascular Dilator Recalled by Galt Medical Corporation Due to The products...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: TVS LPA Recalled by Galt Medical Corporation Due to The products listed...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Smith & Nephew, Inc.

Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...

The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: Centeze Centesis Catheter Recalled by Galt Medical Corporation Due to The...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: 1) ELITE HV Recalled by Galt Medical Corporation Due to The products listed...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: 1) TVS LPA Recalled by Galt Medical Corporation Due to The products listed...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: Elite HV Introducer Recalled by Galt Medical Corporation Due to The products...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Heartware

Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...

The Issue: Possible transient electrical connection interruption between an HVAD System...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 2, 2018· Roche Molecular Systems, Inc.

Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...

The Issue: Cross-contamination of samples has been reported when running the existing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Hobbs Medical, Inc.

Recalled Item: Hobbs Bronchial Cytology Brushes Recalled by Hobbs Medical, Inc. Due to...

The Issue: Device was marketed for uses outside the 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Philips Medical Systems Nederlands

Recalled Item: OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic Recalled by...

The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee MP Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Philips Medical Systems Nederlands

Recalled Item: OmniDiagnost Classic X-ray system Angiographic and Diagnostic Recalled by...

The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing