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. 2,656 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,656 in last 12 months

Showing 42214240 of 51,386 recalls

Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil Recalled by...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Non coated 70 mm Recalled by...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil Recalled by...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CARROLLTON HIP FX Convenience kit used for surgical procedures Recalled by...

The Issue: Products within a Medline pack may be impacted by a packaging error in which...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Recalled by Stryker...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button Recalled...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ARTHROSCOPY Convenience kit used for surgical procedures Recalled by MEDLINE...

The Issue: Products within a Medline pack may be impacted by a packaging error in which...

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

Class II — Potential Health HazardOngoing
FoodOctober 3, 2024· Youngstown Grape Distributors, Inc.

Recalled Item: Happy Moose Juice Strawberry Field packaged in a plastic 12 Recalled by...

The Issue: Incomplete pasteurization

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2024· Youngstown Grape Distributors, Inc.

Recalled Item: Farmers Juice Carrot Digest packaged in a 12 fl. oz. bottle Recalled by...

The Issue: Incomplete pasteurization

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2024· Youngstown Grape Distributors, Inc.

Recalled Item: Happy Moose Juice Tropical Roots packaged in a plastic 12 Recalled by...

The Issue: Incomplete pasteurization

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2024· Youngstown Grape Distributors, Inc.

Recalled Item: Farmers Juice Focus Greens packaged in a 12 fl. oz. bottle Recalled by...

The Issue: Incomplete pasteurization

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2024· Youngstown Grape Distributors, Inc.

Recalled Item: Farmers Juice Watermelon Hydration packaged in a 12 fl. oz. bottle Recalled...

The Issue: Incomplete pasteurization

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing