Medtronic Perfusion Systems DWSClass I

Instruments, Surgical, Cardiovascular

Medtronic Perfusion Systems's record for this product code

MDR events16All time

Recalls1All time

510(k) clearances0All time

Recent MDR events

16 adverse event reports on file

Recalls

1 recall events for this product code

TerminatedNov 1, 2010
Medtronic has received reports regarding the Octopus Nuvo Tissue Stabilizer stating that during use, the collet (a component of the device that stabilizes the head link) fractured, thereby causing immediate separation of the head link from the shaft of the device. The resulting potential hazards are that fragments of the collet could fall into the patient's chest cavity and/or damage the heart ti
View FDA record ↗

510(k) clearances

0 clearances for this product code

No 510(k) clearances on file for Medtronic Perfusion Systems under this product code.