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. 2,547 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,547 in last 12 months

Showing 2156121580 of 51,202 recalls

Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: McGhan Croissant-Shaped Tissue Expanders Recalled by Allergan PLC Due to The...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle Recalled by Allergan PLC Due to The action was initiated following...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle133 Plus Tissue Expander With/Without Suture Tabs Recalled by...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 510 Recalled by Allergan PLC Due to The action was initiated...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Komuro Recalled by Allergan PLC Due to The action was initiated following...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Great Value Mild Taco Seasoning Recalled by CH Guenther & Sons, Inc Due to...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Winco Foods Recalled by CH Guenther & Sons, Inc Due to Potential Salmonella...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: HEB Taco Seasoning Mix 25% Less Sodium Net Wt. 1.25 OZ Recalled by CH...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Williams Ingredients Recalled by CH Guenther & Sons, Inc Due to Potential...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Williams Original Chili Seasoning Recalled by CH Guenther & Sons, Inc Due to...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 23, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Mometasone Furoate Cream USP Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: GMP Deviations: Glenmark received complaints stating that mometasone fuorate...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Revelation with software version VC10 and Biopsy Option Intended...

The Issue: An error can occur when performing a biopsy using the InSpect function. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Recalled by...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· New Standard Device Inc

Recalled Item: 'n'-Hole Post which is a component of the Revolution External Recalled by...

The Issue: The threads on posts stripping out when tensioned during application process.

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

Class II — Potential Health HazardOngoing