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. 2,506 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,506 in last 12 months

Showing 2792127940 of 29,201 recalls

Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT Combo Module Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT Control Module Recalled by Biomerieux Inc Due to...

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT Control Module Recalled by Biomerieux Inc Due to...

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management Recalled by...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Tested AC Control BD Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing