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. 2,469 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,469 in last 12 months

Showing 2382123840 of 28,748 recalls

Medical DeviceSeptember 19, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...

The Issue: GE Healthcare has recently become aware of a potential safety issue to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: MediChoice¿ Multifunction Electrode Part Number: MC171 OH Recalled by...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: Arrow International, Inc. has initiated a voluntary recall for product code...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Intuitive Surgical, Inc.

Recalled Item: EndoWrist Stapler 45 instrument for the da Vinci Si System Recalled by...

The Issue: Intuitive is issuing an urgent product notice to all users of the EndoWrist...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number:...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A Recalled...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer used in conjunction with the da Recalled by...

The Issue: Intuitive Surgical is initiating a voluntary correction relating to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2014· Cooper Vision Caribbean Corp.

Recalled Item: ProClear Toric contact lenses are made from a material containing Recalled...

The Issue: Routine quality monitoring system has identified that a limited number of...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Specimen Transportation System. Product Usage: 10%...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...

The Issue: Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10%...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to...

The Issue: Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10%...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Cardinal Health Prefilled Buffered 10% Formalin. Product Usage:10% NBF is...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Bio-Tite Specimen Containers. Product Usage: 10%...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Specimen Transportation System. 10% NBF is used to...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Protocol 10% NBF Product Usage: 10% NBF is used to Recalled by Richard-Allan...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing