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. 2,457 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,457 in last 12 months

Showing 2736127380 of 28,748 recalls

Medical DeviceNovember 14, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: This notice is being provided in follow up to the field correction initiated...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 13, 2012· Leica Microsystems, Inc.

Recalled Item: Leica ASP6025 Vacuum Tissue Processor The Leica ASP6025 is a Recalled by...

The Issue: The Instruction for Use 1v9 and all previous versions specify incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2012· Medtronic Navigation, Inc.

Recalled Item: The Vertex Max Drill Tube is a component within the Recalled by Medtronic...

The Issue: Medtronic is recalling certain Vertex Max Drill Tubes which are used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2012· Zimmer, Inc.

Recalled Item: Zimmer Spine Ardis Inserter Recalled by Zimmer, Inc. Due to Zimmer Spine has...

The Issue: Zimmer Spine has received reports of the PEEK Ardis Interbody Spacer...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 12, 2012· Greatbatch Medical

Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...

The Issue: Greatbatch Medical observed some anomalies of the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2012· Becton Dickinson & Company

Recalled Item: BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes...

The Issue: BD is conducting a recall of the BD Vacutainer 2.7mL Plus Citrate Blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...

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

Class I — Serious Health HazardOngoing