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. 2,646 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,646 in last 12 months

Showing 1188111900 of 13,548 recalls

DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 9, 2013· Sandoz, Inc

Recalled Item: Ropinirole Recalled by Sandoz, Inc Due to Cross contamination with other...

The Issue: Cross contamination with other products: Sandoz is recalling certain lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2013· Actavis Elizabeth LLC

Recalled Item: Alprazolam Orally Disintegrating Tablets Recalled by Actavis Elizabeth LLC...

The Issue: Failed Tablet/Capsule Specifications; partial tablet erosion resulting in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2013· Amedra Pharmaceuticals LLC

Recalled Item: Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules...

The Issue: Failed Dissolution Specifications: Out of Specification (OOS) test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Slim Fortune capsules Dietary Supplement. Each bottle contains 30 capsules....

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Slim Expert softgel capsules Dietary Supplement. One month supply/ 30...

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Lidiy capsules Dietary Supplement. Each bottle contains 30 capsules....

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 2, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility: Nephron Pharmaceuticals Corporation...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2013· G & W Laboratories Inc

Recalled Item: G & W Fluocinolone Acetonide Cream USP 0.025% Recalled by G & W Laboratories...

The Issue: Failed Content Uniformity Specifications; at the 18 month time point.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: Virilis Pro Recalled by Haute Health, LLC Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: Prolifta Dietary Supplement Prolifta Recalled by Haute Health, LLC Due to...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: PHUK Sexual Enhancement Ultimate Pleasure Recalled by Haute Health, LLC Due...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 26, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: LAMOTRIGINE TABLETS Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: CIPROFLOXACIN TABLETS Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2013· Sandoz Incorporated

Recalled Item: Hydroxychloroquine Sulfate Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Failed Tablet/Capsule Specifications: Sandoz is recalling one lot of...

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

Class III — Low RiskOngoing
Refund