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. 2,474 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,474 in last 12 months

Showing 2246122480 of 28,748 recalls

Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #: 1101 Recalled by...

The Issue: Complaints with the HVAD Retraction of Pins within the driveline connector.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...

The Issue: HeartWare has received complaints relating to damage or bent connection pins...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2015· Richard-Allan Scientific Company

Recalled Item: Mucolytic Agent 1 pint/473 ml Recalled by Richard-Allan Scientific Company...

The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...

The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...

The Issue: Complaints with the HVAD Abnormal Power Source Switching.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· Centurion Medical Products Corporation

Recalled Item: Convenience Kits from Centurion that contain a Medtronic/Covidien Light...

The Issue: Kits from Centurion contain a Medtronic/Covidien Light Glove that is being...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2015· Alcon Research, Ltd.

Recalled Item: The Alcon Custom Pak. The Alcon Customer Pak is an Recalled by Alcon...

The Issue: The supplier of the Devon Light Glove, a component of the Alcon Custom PAK,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: CRIT-LINE Blood Chamber- an accessory to the Crit line III- Recalled by...

The Issue: Blood chamber connection leaks during the use of the CRIT-LINE¿ Blood Chamber

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2015· DeRoyal Industries Inc

Recalled Item: Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves:...

The Issue: Surgical kits contain Medtronic Covidien Devon(TM) Light Gloves which were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2015· GE Healthcare

Recalled Item: D-fend Recalled by GE Healthcare Due to A potential safety issue due to loss...

The Issue: A potential safety issue due to loss of gas monitoring associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: EliteCore Full Core Biopsy Device. EliteCore 18G Recalled by Stryker...

The Issue: Potential for the device cannula to overthrow past the intended length.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr Recalled...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome Precision HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x Recalled by...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x Recalled by...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x Recalled by...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome Precision SI Chronic Catheter Kit 14.5 Fr x 55cm Recalled by...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome HSI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr Recalled...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing