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 2510125120 of 28,748 recalls

Medical DeviceJanuary 9, 2014· Smith & Nephew Inc.

Recalled Item: Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933 Recalled...

The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2014· Smith & Nephew Inc.

Recalled Item: Smith & Nephew RENASYS-G Sterile Recalled by Smith & Nephew Inc. Due to...

The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· OrthoPediatrics Corp

Recalled Item: 3.5mm Locking Cortical Bone Screw Recalled by OrthoPediatrics Corp Due to...

The Issue: OrthoPediatrics has initiated a Voluntary RECALL of Part # 00-0903-2620,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· The Anspach Effort, Inc.

Recalled Item: ANSPACH Cutting bur Recalled by The Anspach Effort, Inc. Due to Anspach...

The Issue: Anspach product code L-3SD contained product code S-3SD which is shorter in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· Veridex, LLC

Recalled Item: CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS...

The Issue: Janssen Diagnostics, LLC received complaints of camera failures on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· B. Braun Medical, Inc.

Recalled Item: SAFSITE¿ Injection Sites and IV Sets manufactured with SAFSITE¿ Injection...

The Issue: Complaints were received reporting leakage on certain lots of SAFSITE¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panaroma Central Station Product Usage: This device can view real time...

The Issue: Mindray has identified two issues with the Panorama Central Station. Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Synthes, Inc.

Recalled Item: Synthes Driving Cap/Threaded Both parts are intended for use in Recalled by...

The Issue: The Synthes Driving Cap/Threaded can bind in the IM Nail Radiolucent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Churchill Medical Systems, Inc.

Recalled Item: AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular...

The Issue: Defective component may cause extension sets to leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Synthes, Inc.

Recalled Item: Drill Template and the Saw Guide for the Ulna Osteotomy Recalled by Synthes,...

The Issue: The Drill Template and the Saw Guide for the Ulna Osteotomy System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Infantino LLC

Recalled Item: Infantino Squeeze & Teethe Monkey Recalled by Infantino LLC Due to Infantino...

The Issue: Infantino initiated this voluntary recall of all lots of Infantino Squeeze &...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing