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. 1,825 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,825 in last 12 months

Showing 3256132580 of 51,386 recalls

FoodOctober 18, 2016· 1 Epic, LLC

Recalled Item: Fruit 66 Strawberry Melon Recalled by 1 Epic, LLC Due to 1 Epic is recalling...

The Issue: 1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 18, 2016· 1 Epic, LLC

Recalled Item: Fruit 66 Mixed Berry Recalled by 1 Epic, LLC Due to 1 Epic is recalling...

The Issue: 1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 18, 2016· 1 Epic, LLC

Recalled Item: Fruit 66 Passion Fruit Mango Recalled by 1 Epic, LLC Due to 1 Epic is...

The Issue: 1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 18, 2016· Teleflex Medical

Recalled Item: Sheridan/CF Recalled by Teleflex Medical Due to Labeling inconsistency -...

The Issue: Labeling inconsistency - units labeled with a 7mm tube may contain a size...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2016· Spacelabs Healthcare Inc

Recalled Item: Xhibit Central Station Recalled by Spacelabs Healthcare Inc Due to The firm...

The Issue: The firm received reports of telemetry SpO2 numerics dropping off the Xhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Covidien LLC

Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...

The Issue: Sterility of the outer surface of the container compromised due to packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Reshape Medical Inc

Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...

The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...

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

Class II — Potential Health HazardOngoing
DrugOctober 13, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Olanzapine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: due to out-of-specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance ICT SP Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
DrugOctober 12, 2016· Pharmedium Services, LLC

Recalled Item: Succinylcholine Chloride Recalled by Pharmedium Services, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: A portion of the batch quantity was...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 12, 2016· Unilever United States, Inc.

Recalled Item: Ben & Jerrys Brownie Batter Core Ice Cream One Pint Recalled by Unilever...

The Issue: Certain pints of Ben & Jerrys Brownie Batter Core Ice Cream may contain...

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

Class II — Potential Health HazardOngoing
Refund