Search Results for: catheter
BD Announces Worldwide Voluntary Recall ofBD Q-Sytea Luer Access Devices and BD Nexiva Closed IV Catheter Systems
Becton, Dickinson and Company is recalling certain lots of BD Q-Syte ™ Luer Access Devices and BD Nexiva ™ Closed IV Catheter Systems. Use of the affected devices may cause an air embolism or leakage of blood and/or therapy, which may result in serious injury or death. This field corrective action included notification to customers worldwide by … [Read more...]
ev3 Endovascular Inc. Trailblazer Support Catheter: Class I Recall
Product Name: Trailblazer Support Catheter Model Numbers SC-014-135, SC-018-090, SC-035-065, SC-035-135, SC-014-150, SC-018-150, SC-035-090, SC-035-150. Lot Numbers 7828282, 7792290, 7792584, 7805570, 7805797, 7806392, 7820252, 7790666, 7791887, 7803307, 7835331, 7822400, 7822593, 7800446, 7800555, 7800756, 7800779, 7800809, 7801822, 7801875, … [Read more...]
Edwards Lifesciences CardioVations EndoClamp Aortic Catheter
Recall Class: Class I Date Recall Initiated: September 24, 2009 Product: CardioVations EndoClamp Aortic Catheter, Model Numbers EC1001 and EC65 This product was manufactured from August, 2008 through August, 2009 and distributed from November, 2008 through September, 2009. Use: The device blocks off the aorta, monitors aortic pressure, … [Read more...]
Neuron 6F 070 Delivery Catheter – Penumbra
Penumbra and FDA notified healthcare professionals about a voluntary field removal of the original version of Neuron 6F 070 Delivery Catheter due to reports that the catheter could kink or ovalize in certain anatomical situations, lead to difficulty in catheter advancement and/or delivery of other devices through the guide catheter. Continued usage … [Read more...]
- « Previous Page
- 1
- 2
- 3
- 4
- 5
- 6
- …
- 10
- Next Page »
Recent Comments