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. 990 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
990 in last 12 months

Showing 31001–31020 of 51,386 recalls

FoodMarch 31, 2017· Pinnacle Foods, LLC

Recalled Item: Great Value Bread and Butter Chips 24 Fl Oz. Distributed by: Wal-Mart Stores...

The Issue: Glass fragments were found in Great Value Bread and Butter Chips.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 31, 2017· Oscor, Inc.

Recalled Item: ATAR Disposable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...

The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 31, 2017· C.R. Bard, Inc.

Recalled Item: Arctic Sun 5000 Temperature Management System Recalled by C.R. Bard, Inc....

The Issue: Potential failure of the Arctic Sun 5000 Temperature Management System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2017· Oscor, Inc.

Recalled Item: ATAR Reusable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...

The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Siemens Medical Solutions USA, Inc.

Recalled Item: 18L6 HD transducer on the ACUSON S Family ultrasound systems Recalled by...

The Issue: When scanning with the 18L6 HD transducer on the ACUSON HELX" Evolution with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Newport Medical Instruments Inc

Recalled Item: Newport Medical HT70 and HT70- Plus Ventilators Recalled by Newport Medical...

The Issue: Medtronic is issuing a voluntary field corrective action for all its...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Rect L Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Knee/Shldr Recalled by Breg Inc Due to They may not have been...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Barco N.V.

Recalled Item: Optional MDRC-1119 Front Cover Attachment Kit for review display monitors....

The Issue: If metal strips are removed and re-applied to another display, there is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Shldr XL Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing