FDA updates guidance on two product recalls

12/2/2010 | MedPage Today (free registration)

The FDA has released new guidance involving two Class I product recalls. In the first guidance, the FDA said the recall of addEASE Binary Connector, made by B. Braun, was caused by stopper fragments that can be released by the device and enter a patient's body, and that distribution and usage of the product should be halted. The second guidance updated the recall of infusion pumps from Baxter Healthcare to a Class I designation.

View Full Article in:

MedPage Today (free registration)

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Catheter Engineer Manager
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
Senior Manager, Compliance
Stryker
Fremont, CA
Director, Office of Device Evaluation
FDA, Center for Devices and Radiological Health
Silver Spring, MD
Director, Office of Compliance
FDA, Center for Devices and Radiological Health
Silver Spring, MD