Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,684 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,684 in last 12 months

Showing 221240 of 13,413 recalls

DrugOctober 14, 2025· FARMAKEIO OUTSOURCING LLC

Recalled Item: Testosterone 200 MG Recalled by FARMAKEIO OUTSOURCING LLC Due to CGMP...

The Issue: CGMP Deviations: Potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 14, 2025· FARMAKEIO OUTSOURCING LLC

Recalled Item: Testosterone / Triamcinolone Acetonide Recalled by FARMAKEIO OUTSOURCING LLC...

The Issue: CGMP Deviations: Potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 14, 2025· FARMAKEIO OUTSOURCING LLC

Recalled Item: Testosterone Regular Release 200 MG Recalled by FARMAKEIO OUTSOURCING LLC...

The Issue: CGMP Deviations: Potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 14, 2025· FARMAKEIO OUTSOURCING LLC

Recalled Item: Testosterone 87.5 MG Recalled by FARMAKEIO OUTSOURCING LLC Due to CGMP...

The Issue: CGMP Deviations: Potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· Alembic Pharmaceuticals Limited

Recalled Item: Fesoterodine Fumarate Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Failed Impurities/Degradation Specifications: Due to levels of 'Diester...

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

Class III — Low RiskOngoing
Refund
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 7.5mg Recalled by Endo USA, Inc. 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
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 2.5 mg Recalled by Endo USA, Inc. 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
DrugOctober 10, 2025· QuVa Pharma, Inc.

Recalled Item: R.E.C.K. (Ropivacaine HCl Recalled by QuVa Pharma, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 10 mg Recalled by Endo USA, Inc. 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
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 5mg Recalled by Endo USA, Inc. 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
DrugOctober 10, 2025· Lannett Company Inc.

Recalled Item: Niacin Extended-release Tablets Recalled by Lannett Company Inc. Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Failed...

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
DrugOctober 10, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Failed...

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
DrugOctober 9, 2025· STAQ Pharma, Inc.

Recalled Item: Ketamine Hydrochloride Recalled by STAQ Pharma, Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2025· USV Private Limited

Recalled Item: Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % Recalled by USV...

The Issue: Failed Impurities/Degradation Specifications: The result for 'Any individual...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2025· Amerisource Health Services LLC

Recalled Item: Sucralfate Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: The recalling firm filed for Chapter 11 on September 30,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2025· STAQ Pharma, Inc.

Recalled Item: Hydromorphone HCL PF Recalled by STAQ Pharma, Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2025· STAQ Pharma, Inc.

Recalled Item: FentaNYL Citrate PF Recalled by STAQ Pharma, Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugOctober 8, 2025· Mohamed Hagar

Recalled Item: Mojo Max Fusion XXX Recalled by Mohamed Hagar Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared...

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

Class I — Serious Health HazardOngoing
Refund