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. 2,497 recalls have been distributed to Kentucky in the last 12 months.
Showing 20401–20420 of 28,748 recalls
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liver Access and Biopsy Needle Set Biopsy needle kit Intended Recalled by...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Torcon NB Advantage Catheter Catheter Recalled by Cook Inc. Due...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selective Salpingography Catheter with Beacon Tip Cannula Recalled by Cook...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Lower Back Garment Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slip-Cath Beacon Tip Catheter Catheter Recalled by Cook Inc. Due to Increase...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FluoroSet Radiographic Tubal Assessment Set Cannula Recalled by Cook Inc....
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter Catheter Recalled by Cook...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transluminal Biliary Biopsy Forceps Set Forceps Recalled by Cook Inc. Due to...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentaray NAV High-Density Mapping ECO Catheter Recalled by Biosense Webster,...
The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium on RX Imola analyser IVD Recalled by Randox Laboratories, Limited...
The Issue: According to the firm, Carry over was observed when the amylase or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEXL-3010/A5- Vantage Titan 3T Magnetic Resonance Imaging System Product...
The Issue: A potential problem associated to the gradient coil (ASGC) in the Titan 3T...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite...
The Issue: BBMI recently identified a potential for a tear in the outer blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Vented Dispensing Pin with Luer Lock Ultrasite Valve Product Usage:...
The Issue: BBMI recently identified a potential for a tear in the outer blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentaray NAV High-Density Mapping Catheter Recalled by Biosense Webster,...
The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Dynamics Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has identified changes in default carry forward workflow using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.