Search Tag: Teleflex
2015 29 Jun
Teleflex Incorporated announced today that the U.S. Food and Drug Administration (FDA) has classified the voluntary medical device recall of Hudson RCI® LIFESAVER® Neonate Manual Resuscitator as a Class 1 recall. FDA defines Class I recalls as, “a situation in which there is a reasonable probability that the use of or exposure to a violative product...Read more
2013 04 Jun
Teleflex Incorporated, a leading global provider of medical devices for critical care, urology and surgery, will showcase its comprehensive anesthesia portfolio, including regional anesthesia, at the Euroanaesthesia congress in Barcelona, Spain on June 1-4, 2013. At the ESA congress on June 1-4, Teleflex unveils the broadening...Read more