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 19011920 of 51,386 recalls

FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Lowfat Yogurt with Toppers Two-product package. Contains 8-6oz...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Low Fat Yogurt with toppers. Vanilla with Oreo cookie pieces...

The Issue: Foreign material (plastic)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Lowfat Yogurt with Toppers. Two-product packages. 1. Contains 8-...

The Issue: Foreign material (plastic pieces)

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

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
Medical DeviceJuly 11, 2025· Onkos Surgical, Inc.

Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...

The Issue: Unidentified substance of unknown impact was identified on devices during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2025· Onkos Surgical, Inc.

Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...

The Issue: Unidentified substance of unknown impact was identified on devices during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2025· Onkos Surgical, Inc.

Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...

The Issue: Unidentified substance of unknown impact was identified on devices during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2025· ICU Medical, Inc.

Recalled Item: Plum Duo Infusion System Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical identified two sequences of programming events and alarm...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: BritePro Solo Single-Use Fiber Optic Mini Handle and Blade by Flexicare...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: BritePro Solo Mini with Pro Miller Blade Size 1.5 Recalled by Flexicare...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: BritePro Solo Single-Use Fiber Optic Laryngoscope Handle :040-310AU and...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle Recalled by...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: BritePro Solo Single-Use Fiber Optic Handle and Blade : 040-331U (Mac 1)...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle Recalled by...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Remel, Inc

Recalled Item: Blood Agar Recalled by Remel, Inc Due to Potential Listeria Contamination

The Issue: The products may contain surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing