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
Diagnostic Technician
Roche
Marlborough, MA
Test Technician
Roche
Marlborough, MA
Compliance and Ethics Director
Sysmex America, Inc.
Lincolnshire, IL
Director, Site Quality Management
CareFusion
Palm Springs, CA
Compliance Officer-Medical Products
W. L. Gore
Flagstaff, AZ