Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,672 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,672 in last 12 months

Showing 421440 of 13,398 recalls

DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Methylene Blue for Injection Recalled by GenoGenix LLC Due to Lack of...

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
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: NAD+ (Nicotinamide adenine dinucleotide) Recalled by GenoGenix LLC Due to...

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
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: N-Acetyl-L-Cysteine for Injection Recalled by GenoGenix LLC Due to Lack of...

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
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: L-Carnitine for Injection Recalled by GenoGenix LLC Due to Lack of Assurance...

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
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Cerebrolysin for Injection Recalled by GenoGenix LLC Due to Lack of...

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
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Magnesium Chloride for Injection Recalled by GenoGenix LLC Due to Lack of...

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
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: GHK-Cu (Copper Peptide) for Injection Recalled by GenoGenix LLC Due to Lack...

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
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Glycine for Injection Recalled by GenoGenix LLC Due to Lack of Assurance of...

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
DrugJuly 29, 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 in September 2024....

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2025· Alembic Pharmaceuticals Limited

Recalled Item: Doxepin Hydrochloride Capsules Recalled by Alembic Pharmaceuticals Limited...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2025· Cipla USA, Inc.

Recalled Item: Albuterol Sulfate Recalled by Cipla USA, Inc. Due to Failed Stability...

The Issue: Failed Stability Specifications: Out of specification results was observed...

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

Class III — Low RiskOngoing
Refund
DrugJuly 22, 2025· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An out-of-Specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2025· Ascend Laboratories, LLC

Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories,...

The Issue: Failed Dissolution Specifications: low dissolution results

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2025· Merck & Co. Inc

Recalled Item: Belsomra (suvorexant) tablets Recalled by Merck & Co. Inc Due to Failed...

The Issue: Failed Dissolution Specifications: potential for delayed dissolution of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2025· DermaRite Industries, LLC

Recalled Item: KleenFoam Recalled by DermaRite Industries, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 17, 2025· DermaRite Industries, LLC

Recalled Item: DermaKleen Recalled by DermaRite Industries, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 17, 2025· DermaRite Industries, LLC

Recalled Item: DermaSarra Recalled by DermaRite Industries, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 17, 2025· DermaRite Industries, LLC

Recalled Item: PeriGiene Recalled by DermaRite Industries, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 15, 2025· Breckenridge Pharmaceutical, Inc.

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

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2025· Nostrum Laboratories, Inc.

Recalled Item: Sucralfate Tablets Recalled by Nostrum Laboratories, Inc. Due to CGMP...

The Issue: CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024....

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

Class II — Potential Health HazardOngoing
Refund