Important Safety Alerts

The United States Food and Drug Administration (FDA) posted a medical device safety alert concerning components of MAQUET Servo Humidifier 163 [Lot numbers: 201413, 201414, 201415, 201417, 201419 and 201422], manufactured by Teleflex Medical Inc.

The recall was initiated because of cracks that may occur in the center of the corrugated flex tube of the 15 mm and 22 mm ISO female connector.

For details, please refer to the following FDA website:

http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1051-2015&w=02182015&lang=eng

If you are in possession of the affected products, please contact your supplier for necessary actions.

Posted on 23 February 2015