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 1172111740 of 13,548 recalls

DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Oil EAR DROPS Recalled by...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS DermOtic Oil fluocinolone acetonide 0.01% (Ear Drops)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops Recalled by Hill...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil (Body Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% (Scalp...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2014· Caraco Pharmaceutical Laboratories Ltd.

Recalled Item: Oxcarbazepine Tablets Recalled by Caraco Pharmaceutical Laboratories Ltd....

The Issue: Failed Tablet Specifications: Broken Tablets Present.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Cream USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Labeling: Label Error on Declared Strength: There is a misprint on the end...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2014· Pfizer Inc.

Recalled Item: GREENSTONE BRAND fluconazole for Oral Suspension Recalled by Pfizer Inc. Due...

The Issue: Defective Container: Tamper evident ring failures discovered on some bottles.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 28, 2014· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Carisoprodol Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurity/degradation Specification

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

Class III — Low RiskOngoing
Refund
DrugJanuary 28, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by Caraco Pharmaceutical...

The Issue: Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2014· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product did not meet...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2014· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product did not meet...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: REDUCE WEIGHT FRUTA PLANTA Capsules Recalled by MyNicNaxs, Inc. Due to...

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
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Magic Slim capsules Recalled by MyNicNaxs, Inc. Due to Undeclared Active

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
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Slim Xtreme Weight loss capsules Recalled by MyNicNaxs, Inc. Due to...

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
DrugJanuary 24, 2014· Teva Pharmaceuticals USA

Recalled Item: Teva Hydroxyzine Pamoate Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: CGMP Deviations: Hydroxyzine Pamoate Capsules, USP, 100 mg were manufactured...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2014· Teva Pharmaceuticals USA

Recalled Item: Teva Hydroxyzine Pamoate Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: CGMP Deviations: Hydroxyzine Pamoate Capsules, USP, 25 mg were manufactured...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: SlimEasy Herbs Capsule Recalled by MyNicNaxs, Inc. Due to Undeclared Active

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