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. 2,700 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,700 in last 12 months

Showing 37613780 of 13,548 recalls

DrugSeptember 27, 2021· AMIVAS (US), LLC

Recalled Item: Artesunate for Injection Recalled by AMIVAS (US), LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: Air filter failed post integrity test...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2021· Strides Pharma Inc.

Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by Strides Pharma Inc....

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2021· Eli Lilly & Company

Recalled Item: Glucagon Emergency Kit for Low Blood Sugar Recalled by Eli Lilly & Company...

The Issue: SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Recalled Item: Testosterone Cypionate Testosterone Propionate Recalled by New Vitalis...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2021· SigmaPharm Laboratories LLC

Recalled Item: Sodium Phenylbutyrate Powder Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Failed Impurities/Degradation Specifications; Out of Specification impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2021· Fresenius Kabi USA LLC

Recalled Item: Morphine Sulfate Injection Recalled by Fresenius Kabi USA LLC Due to...

The Issue: Defective container: Cracked vials leading to lack of sterility assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2021· American Health Packaging

Recalled Item: GlipiZIDE Extended-Release Tablets Recalled by American Health Packaging Due...

The Issue: Failed Dissolution Specifications: results were above specification.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2021· American Health Packaging

Recalled Item: Valproic Acid Oral Solution Recalled by American Health Packaging Due to...

The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2021· Viatris

Recalled Item: Candesartan Cilexetil Tablets Recalled by Viatris Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 10, 2021· Piramal Critical Care, Inc.

Recalled Item: Rocuronium Bromide Injection 50mg/5 mL Recalled by Piramal Critical Care,...

The Issue: Labeling: Label Lacks Warning or Rx Legend: Finished product did not include...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2021· Vi-Jon, Inc.

Recalled Item: Kroger 70% Isopropyl Alcohol First Aid Antiseptic 32 FL OZ Recalled by...

The Issue: Labeling: Label Mix-Up.The recall has been initiated after receiving one...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2021· Aurobindo Pharma USA Inc.

Recalled Item: Metoprolol Tartrate Tablets USP 100 mg Recalled by Aurobindo Pharma USA Inc....

The Issue: Presence of Foreign Substance: Product complaints received for the presence...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 8, 2021· Akorn, Inc.

Recalled Item: TheraTears Extra (sodium carboxymethylcellulose) 0.25% Lubricant Eye Drops...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2021· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Promethazine Syrup Plain Recalled by Morton Grove Pharmaceuticals, Inc. Due...

The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2021· Meitheal Pharmaceuticals Inc

Recalled Item: Glycopyrrolate Injection Recalled by Meitheal Pharmaceuticals Inc Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund