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. 1,137 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,137 in last 12 months

Showing 1101–1120 of 51,386 recalls

Medical DeviceOctober 3, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: TruDi¿ Navigation System - Multi Instrument Adapter Recalled by Integra...

The Issue: It was determined that when the navigation system is configured with...

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

Class II — Potential Health HazardOngoing
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Food Club Finely Shredded Pizza Style Four Cheese Blend (containing Recalled...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Pizza style shredded cheese blend (containing low-moisture part-skim...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Italian style shredded cheese blend (containing low-moisture part-skim...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Good & Gather Mozzarella & Parmesan shredded cheese blend Recalled by Great...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Happy Farms by Aldi Italian Style shredded cheese blend (containing Recalled...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Mozzarella and provolone shredded cheese blend (containing low-moisture...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Low-moisture part-skim mozzarella shredded cheese Recalled by Great Lakes...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2025· ICU Medical, Inc.

Recalled Item: IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave Recalled by...

The Issue: IV Gravity burette administration set burette component is missing an...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 2, 2025· Cerenovus Inc

Recalled Item: CEREPAK Detachable Coil System - Name/ 2MM X 2.5 CM/FCX100202 Recalled by...

The Issue: Detachable coils system may fail to detach, which could result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 2, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model...

The Issue: The motorized longitudinal movement of the FlexArm stand may be inconsistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Philips Medical Systems DMC GmbH

Recalled Item: DigitalDiagnost 4 (1) High Performance Recalled by Philips Medical Systems...

The Issue: Philips has identified that some ceiling suspension telescopic carriages...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated Recalled by...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Philips Medical Systems DMC GmbH

Recalled Item: Precision CRF Recalled by Philips Medical Systems DMC GmbH Due to Philips...

The Issue: Philips has identified that some ceiling suspension telescopic carriages...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated Recalled by...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated Recalled by...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Philips Medical Systems DMC GmbH

Recalled Item: DigitalDiagnost C90 (1) High Performance Recalled by Philips Medical Systems...

The Issue: Philips has identified that some ceiling suspension telescopic carriages...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal LigaSure Small Jaw Instrument (Purple/White) Recalled by...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Philips Medical Systems DMC GmbH

Recalled Item: Radiography 7300 C Recalled by Philips Medical Systems DMC GmbH Due to...

The Issue: Philips has identified that some ceiling suspension telescopic carriages...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal LigaSure Blunt Tip Sealer/Divider Recalled by Medline...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing