FDA classifies Teleflex's IV recall as Class I

04/10/2010 | Clinica (subscription required)

The FDA has classified the recall of Teleflex's intravenous tubing sets and accessories, which are used for transferring fluids into a patient's blood vessels, as a Class I recall. The recall was prompted by the finding of holes in the packaging that could lead to "blood-borne or other types of infections, which could result in serious injury or death."

View Full Article in:

Clinica (subscription required)

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Food & Drug Associate
Confidential
Washington, D.C., DC
Senior Manager, Gaps in Care
UAW Retiree Medical Benefits Trust
Detroit, MI
Compliance Director
Abbott Laboratories
Santa Clara, CA
Product Development Manager, Disposable Medical Products
ASAHI INTECC, Orange County CA R&D Center
Santa Ana, CA
Neurovascular Intervention Product Sales Rep, North East
ASAHI INTECC
Multiple Locations, SL_Multiple Locations