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 28812900 of 51,386 recalls

Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Cross Contamination

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Cross Contamination

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Tolterodine Tartrate Extended-Release Capsules Recalled by The Harvard Drug...

The Issue: Failed Dissolution Specifications: Out of specification results obtained...

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· Chattem Inc

Recalled Item: Unisom Recalled by Chattem Inc Due to CGMP Deviations: Nitrosamine Drug...

The Issue: CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Medtronic Neuromodulation

Recalled Item: Stimulation RC Clinician Programmer Application Recalled by Medtronic...

The Issue: There is a software issue that can permanently disable communication with an...

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

Class II — Potential Health HazardOngoing
FoodMarch 3, 2025· U.S. Tov, Inc. dba U.S. Trading Company

Recalled Item: DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily Recalled by...

The Issue: Undeclared sulfites

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) NAIL PACK Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) ED CRASH Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: to RES Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to There is a...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) CW PERI GYN...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) T&A ENDO PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing