FDA MedWatch-Terumo Cardiovascular Systems Tenderflow Pediatric Arterial Cannulae- Recalled due to reports of difficulty retracting the introducer from the cannula

[Date Prev][Date Next][Thread Prev][Thread Next][Date Index][Thread Index]

 



Title: FDA MedWatch-Terumo Cardiovascular Systems Tenderflow Pediatric Arterial Cannulae- Recalled due to reports of difficulty retracting the introducer from the cannula
MedWatch logo MedWatch - The FDA Safety Information and Adverse Event Reporting Program

Terumo Cardiovascular Systems notified healthcare professionals of a worldwide recall of its Tenderflow Pediatric Arterial Cannulae involving 21 lot codes (see Terumo press release for complete list). Terumo received five reports of difficulty retracting the introducer from the cannula. When the introducer cannot be retracted from the cannula, the cannula must be removed and replaced, a process that may lead to aortic damage, blood loss and/or death. Healthcare professionals are advised to not use the product unless medically necessary. In those cases, the cannula should be used without the introducer.

Read the MedWatch 2008 safety summary, including a link to the firm press release, at:

http://www.fda.gov/medwatch/safety/2008/safety08.htm#Tenderflow


Update your subscriptions, modify your e-mail address, or stop subscriptions at any time on your Subscriber Preferences Page. You will need to use your e-mail address to log in. If you have questions or problems with the subscription service, please contact support@xxxxxxxxxxxxxxx.

This service is provided to you at no charge by U.S. Food & Drug Administration (FDA).

FDA HHS

GovDelivery, Inc. sending on behalf of U.S. Food & Drug Administration (FDA) · 5600 Fishers Lane · Rockville MD 20857 · 800-439-1420


[Index of Archives]     [CDC News]     [NIH News]     [USDA News]     [Steve's Art]     [Camping in Yosemite]     [PhotoForum]     [SB Lupus]     [STB]

  Powered by Linux