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. 2,716 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,716 in last 12 months

Showing 26412660 of 13,548 recalls

DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Dakin's Solution Recalled by Mckesson Medical-Surgical Inc. Corporate Office...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Alcohol Swabsticks Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Eye-stream Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Triple Antibiotic Ointment Recalled by Mckesson Medical-Surgical Inc....

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Telmisartan and Hydrochlorothiazide Tablets USP Recalled by Glenmark...

The Issue: Defective Container: Recall of these batches has been initiated due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Naphcon A eye drops Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Bisacodyl Suppositories Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Systane Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Systane Balance Recalled by Mckesson Medical-Surgical Inc. Corporate Office...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Debrox Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: A&D Original Ointment Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Testosterone Gel 1% (25mg testosterone/2.5g of gel) 2.5 g per unit dose...

The Issue: Superpotent Drug: Out of specification assay result was obtained during...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Aspirin and Extended-Release Dipyridamole Capsules Recalled by Glenmark...

The Issue: Failed Tablet/Capsule Specification : Capsule breakage

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2022· Vi-Jon, LLC

Recalled Item: Hydrogen Peroxide Topical Solution USP Recalled by Vi-Jon, LLC Due to Cross...

The Issue: Cross Contamination With Other Products: Product is cross contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: Failure occurred during routine stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...

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
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Undeclared...

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
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...

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
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

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

Class II — Potential Health HazardOngoing
Refund