Wednesday, September 15, 2010

Westmed, Inc. Issues Nationwide Recall of BagEasy Manual Resuscitation Devices

Westmed, Inc. Issues Nationwide Recall of BagEasy Manual Resuscitation Devices
Wed, 15 Sep 2010 14:46:00 -0500

Westmed, Inc., Tucson, AZ, is initiating a nationwide recall of 24,384 units of BagEasy Manual Resuscitation Devices. The select lots listed below of the BagEasy device have been found to have a potential for disconnection at the retention ring of the patient port manifold.


Manage your FDA Subscriptions:

U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420

No comments:

Post a Comment