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. 1,727 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,727 in last 12 months

Showing 4896148980 of 51,202 recalls

Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· Brookstone Company, Inc.

Recalled Item: Brookstone Heated Body Bean Recalled by Brookstone Company, Inc. Due to...

The Issue: Additional Warning Statement to prevent burns to the skin

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· California Medical Laboratories Inc

Recalled Item: Rigid Tip Suction Wand Non sterile bulk devices (S112468N Recalled by...

The Issue: California Medical Laboratories, Inc. has identified an issue with the Rigid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· California Medical Laboratories Inc

Recalled Item: Sterile Rigid Tip Suction Wand The Suction Wands are indicated Recalled by...

The Issue: California Medical Laboratories, Inc. has identified an issue with the Rigid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
DrugNovember 2, 2012· Bristol Myers Squibb Manufacturing Company

Recalled Item: ABILIFY (aripiprazole) Tablets Recalled by Bristol Myers Squibb...

The Issue: CGMP Deviations: A drum of Abilify 30 mg Tablets rejected during the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2012· Biomet, Inc.

Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 13.0 thru 20.0 Recalled by Biomet, Inc....

The Issue: Biomet has initiated this action following an investigation which identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Operations,...

The Issue: On cobas c 701 and cobas c 702 modules of the Cobas 8000 series analyzer, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Biomet, Inc.

Recalled Item: Bio-Modular Humeral Head 48mm x 24mm Ti 6AI4V/Ion Implanted (Orthopedic...

The Issue: The items in this lot are missing the ion implantation feature. The surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Biomet, Inc.

Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 8.0 THRU 12.5 Recalled by Biomet, Inc....

The Issue: Biomet has initiated this action following an investigation which identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Beckman Coulter Inc.

Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to It has...

The Issue: It has been determined that, in some cases, pulley drive components have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B...

The Issue: Ortho Clinical Diagnostics is recalling certain lots of the Vitros Anti-HBs...

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

Class III — Low RiskOngoing
Medical DeviceNovember 1, 2012· Merge Healthcare, Inc.

Recalled Item: CADstream software. Product Usage: CADstream is an image processing system...

The Issue: An incorrect biopsy or missed target could result if the incorrect grid is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: This notice is being provided in follow up to the field correction initiated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2012· Hill-Rom, Inc.

Recalled Item: Liko Overhead Rail System Recalled by Hill-Rom, Inc. Due to Liko/Hill-Rom to...

The Issue: Liko/Hill-Rom to date has received two reports from facilities alleging that...

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

Class II — Potential Health HazardOngoing