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. 2,509 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,509 in last 12 months

Showing 1854118560 of 28,748 recalls

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· 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· 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· 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: If Hip Recalled by Breg Inc Due to They may not have been sealed prior to...

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· Breg Inc

Recalled Item: Dressing M/U 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
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 Back 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· Breg Inc

Recalled Item: Dressing Shldr 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· 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 29, 2017· Stryker Medical Division of Stryker Corporation

Recalled Item: Medi-Therm Hyper/Hypothermia System Recalled by Stryker Medical Division of...

The Issue: The water may reheat too quickly if the unit is in "Automatic" mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2017· Teleflex Medical

Recalled Item: Arrow EZ-IO Needle Set 45 mm 15 ga Recalled by Teleflex Medical Due to Some...

The Issue: Some of the individual unit packaging (pouches) may be missing the lot...

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

Class III — Low RiskOngoing