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. 1,099 recalls have been distributed to Kentucky in the last 12 months.
Showing 9001–9020 of 51,386 recalls
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers - intended to Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be Recalled...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-PRO 2- A powered ambulance cot that consists of a platform Recalled by...
The Issue: Base leg assembly may bend and result in difficulty engaging/disengaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RET Proximal Probe. Used in Fluorescence in situ hybridization (FISH)...
The Issue: DNAs used during the manufacture of two affected models were accidentally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RET Distal Probe. Used in Fluorescence in situ hybridization (FISH) Recalled...
The Issue: DNAs used during the manufacture of two affected models were accidentally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.