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. 2,634 recalls have been distributed to Kentucky in the last 12 months.
Showing 7481–7500 of 28,748 recalls
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IgM Immunoturbidimetric Assay-In vitro determination of IgA and IgM in...
The Issue: Update to the carryover avoidance technical bulletin to detail that IgA and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IgA Immunoturbidimetric Assay- In vitro determination of IgA and IgM...
The Issue: Update to the carryover avoidance technical bulletin to detail that IgA and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak Surgical Procedure Pack Recalled by Alcon Research, LLC Due...
The Issue: Due to difficulty removing the liner on the adhesive components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0. Used to display medical images (Including...
The Issue: There is the potential that after installation of the IAS tool, some studies...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0. Used to display...
The Issue: There is the potential that after installation of the IAS tool, some studies...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit Recalled by...
The Issue: There is the potential for inadequate connection between the top and bottom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr...
The Issue: There is the potential for inadequate connection between the top and bottom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE Recalled by...
The Issue: Upon review of its batch record, Southmedic identified that lot # W92761 was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic...
The Issue: Confirmed an average positive bias of 40% for testosterone concentrations of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GREER M. FAENI Recalled by Greer Laboratories, Inc. Due to The product was...
The Issue: The product was recalled because stability evaluation of the lots indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GREER DIA - KIT ANTIGEN M. FAENI Recalled by Greer Laboratories, Inc. Due to...
The Issue: The product was recalled because stability evaluation of the lots indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrackX Insight Base Modular Instrument Tracker Recalled by Trackx Technology...
The Issue: The device is breaking and falling off the Nuvasive T-Handle with Hudson...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...
The Issue: The products may have the potential to burn customers. Firm has received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...
The Issue: The products may have the potential to burn customers. Firm has received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.