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 28212840 of 51,386 recalls

DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Nitroglycerin Sublingual Tablets 0.3MG Recalled by Glenmark Pharmaceuticals...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Lacosamide Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Propafenone Hydrochloride Extended-Release Capsules 225mg Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Voriconazole Tablets 200 mg Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Solifenacin Succinate Tablets 10MG Recalled by Glenmark Pharmaceuticals...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Teriflunomide Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Fluphenazine Hydrochloride Tablets 2.5mg Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 13, 2025· Thoratec LLC

Recalled Item: HeartMate Mobile Power Unit: Recalled by Thoratec LLC Due to Left...

The Issue: Left Ventricular Assist System Mobile Power Unit (MPU) may have electrical...

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

Class I — Serious Health HazardOngoing
FoodMarch 12, 2025· FRUSELVA USA

Recalled Item: Good & Gather baby Pea Recalled by FRUSELVA USA Due to elevated level of lead

The Issue: elevated level of lead

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2025· Alchemee, LLC

Recalled Item: Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%) Recalled by...

The Issue: Chemical contamination: Presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2025· Alchemee, LLC

Recalled Item: Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%) Recalled by...

The Issue: Chemical contamination: Presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2025· Qiagen Sciences LLC

Recalled Item: Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus...

The Issue: Identified faulty cartridges. If such a faulty cartridge is used for sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number:...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Recalled by...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
FoodMarch 11, 2025· C.H. Guenther & Son LLC

Recalled Item: 365 Whole Foods Market Small Bites Macaroni & Cheese. Net Recalled by C.H....

The Issue: Undeclared allergen (eggs) and pork

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

Class I — Serious Health HazardOngoing
Refund