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

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: 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.

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