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. 1,976 recalls have been distributed to Kentucky in the last 12 months.
Showing 13021–13040 of 28,748 recalls
Recalled Item: Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System...
The Issue: The firm became aware of a cleaning solution leaking issue from the middle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...
The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK Hem-O-Lok AutoEndo5 Recalled by Teleflex Medical Due to Certain clip...
The Issue: Certain clip appliers have an increase in misloading and/or jamming related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Homocysteine-In vitro test for the quantitative determination of total...
The Issue: Homocysteine Reagent, Calibration Failures and Quality Control Recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: Device may fail to turn on or unexpectedly attempt to restart, rendering it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 440mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft Recalled by Ethicon...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4mm x 2.5 Fluted Pin Pouch Recalled by Exactech, Inc. Due to Potential for...
The Issue: Potential for the 2.4mm x 2.5 Fluted Pin Pouch to contain a single pin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCFE (slipped capital femoral epiphysis) Knobs for Driver Recalled by Pega...
The Issue: There is a potential for the screws to have become loosened during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Component for Laser Scanning Microscopes (LSM 700 Recalled by Zeiss, Carl...
The Issue: When the user tilts the transmitted light arm of the microscope to the end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.