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. 2,721 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,721 in last 12 months

Showing 120 of 51,202 recalls

DrugMarch 9, 2026· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Icosapent Ethyl Capsules Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Failed Tablet/Capsule specifications: Red dots inside capsule and melted...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2026· Rising Pharma Holding, Inc.

Recalled Item: Product label: Temozolomide Capsules Recalled by Rising Pharma Holding, Inc....

The Issue: Failed Impurities/Degradation Specifications: An out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2026· MYLAN PHARMACEUTICALS INC

Recalled Item: Isotretinoin Capsules Recalled by MYLAN PHARMACEUTICALS INC Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2026· Cipla USA, Inc.

Recalled Item: Nilotinib Capsules Recalled by Cipla USA, Inc. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: Observed OOS results at 6-months...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 18, 2026· HTO Nevada Inc. dba Kirkman

Recalled Item: FIVE-STAR Recalled by HTO Nevada Inc. dba Kirkman Due to Stability Data Does...

The Issue: Stability Data Does Not Support Expiry Date.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2026· HTO Nevada Inc. dba Kirkman

Recalled Item: MAXIMUM Recalled by HTO Nevada Inc. dba Kirkman Due to Stability Data Does...

The Issue: Stability Data Does Not Support Expiry Date.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2026· HTO Nevada Inc. dba Kirkman

Recalled Item: MAXIMUM Recalled by HTO Nevada Inc. dba Kirkman Due to Stability Data Does...

The Issue: Stability Data Does Not Support Expiry Date.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2026· Cipla USA, Inc.

Recalled Item: Nilotinib Capsules Recalled by Cipla USA, Inc. Due to Failed Tablet/Capsule...

The Issue: Failed Tablet/Capsule Specifications: Observed OOS results at 6-months...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2026· The Harvard Drug Group LLC

Recalled Item: Midodrine Hydrochloride Tablets Recalled by The Harvard Drug Group LLC Due...

The Issue: Defective container; inadequately sealed blister packaging.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 13, 2026· Ambrosia Brands LLC

Recalled Item: Rosabella brand MORINGA Recalled by Ambrosia Brands LLC Due to Potential...

The Issue: Product may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2026· Harbin Jixianglong Biotech Co., Ltd.

Recalled Item: Semaglutide Recalled by Harbin Jixianglong Biotech Co., Ltd. Due to CGMP...

The Issue: CGMP Deviations This recall has been initiated due to failing to complete...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2026· Harbin Jixianglong Biotech Co., Ltd.

Recalled Item: Semaglutide Recalled by Harbin Jixianglong Biotech Co., Ltd. Due to CGMP...

The Issue: CGMP Deviations This recall has been initiated due to failing to complete...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2026· AvKARE

Recalled Item: Amantadine HCl Recalled by AvKARE Due to Failed Dissolution Specifications:...

The Issue: Failed Dissolution Specifications: This recall has been initiated due to an...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2026· Slate Run Pharmaceuticals

Recalled Item: Eptifibatide Injection Recalled by Slate Run Pharmaceuticals Due to...

The Issue: Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 10, 2026· LEO PHARMA INC

Recalled Item: Adbry Recalled by LEO PHARMA INC Due to Lack of Assurance of Sterility: due...

The Issue: Lack of Assurance of Sterility: due to the presence of particulate matter in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2026· Boston Scientific Corporation

Recalled Item: EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to...

The Issue: Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or...

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

Class II — Potential Health HazardOngoing
DrugFebruary 9, 2026· Meitheal Pharmaceuticals, Inc

Recalled Item: Cetrorelix Acetate for Injection (Kit) Recalled by Meitheal Pharmaceuticals,...

The Issue: Defective Delivery System: Missing or duplicated needles within the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· International Life Sciences

Recalled Item: Artelon FlexBand Dynamic Matrix Recalled by International Life Sciences Due...

The Issue: Augmentation devices failed bacterial endotoxin testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing