Mindray initiates voluntary recall for A3/A5 Anesthesia Delivery System

Published on November 14, 2012 at 12:14 AM · No Comments

Mindray has advised the US Food and Drug Administration of this voluntary recall.

Any adverse reactions or quality problems experienced with the use of this product may be reported to the U.S. Food and Drug Administration's (FDA) MedWatch Adverse Events Program either online, by regular mail or by fax.

SOURCE Mindray Medical International Limited

Posted in: Device / Technology News

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