BagEasy manual resuscitation devices are used for patients requiring complete or intermittent ventilatory support. It can provide positive pressure ventilation or oxygen for the spontaneously breathing patient with a face mask or through an artificial airway. A manual emergency ventilator is a device, incorporating a bag and valve, intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway.
FDA Recall Z-2333-2010 · Posted 2010-09-08
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Recalling FirmWestmed Inc
Recall StatusTerminated
Product CodeBTM
Date Initiated2010-06-22
Date Terminated2011-03-22
Product Quantity2,734
Reason for Recall
This recall was initiated after Westmed, Inc. became aware of a potential for disconnection at the patient port retention ring assembly of the Bag Easy manual resuscitation device.
Firm Action
The firm, Westmed, sent a letter dated June 21, 2010, to all customers. The letter describes the product, problem and action to be taken by customer. The customers were instructed to cease distribution immediately, notify any facilities that they may have distributed the product identified of the recall, call Customer Service Manager at 1-800-975-7987 x 1223 and/or email [email protected] to receive Return Authorization to return identified product, and complete and return the enclosed Bag Easy Recall Reconciliation Checklist.
If you have any question, contact Customer Service at 1-800-975-7987 or 1-520-294-7987.
Root Cause
Nonconforming Material/Component
Distribution Pattern
Worldwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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