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. 2,417 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,417 in last 12 months

Showing 4908149100 of 51,202 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 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 BacT/ALERT 3D 60 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 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
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Acne Astringent Toner Pads (salicylic acid 2% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Severe Maximum Strength Acne Pore Cleanser (benzoyl peroxide 5%...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Original Strength Terminator (benzoyl peroxide 5% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree 24 Hour Clearing System containing 1-count 4 fl oz Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Oil-Free Acne Cleanser (benzoyl peroxide 2.5% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree 24 Hour Severe Acne Clearing System containing 1-count 4 Recalled...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund