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Mindray DS USA, Inc. dba Mindray North America recalls A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general inhal
Recalled September 7, 2016 · FDA recall Z-2689-2016 · Mindray DS USA, Inc.
Hazard
Potential for a leak to occur on the back-up O2 and air e-size cylinder yokes on the A7 Anesthesia Delivery System. · FDA Class II
Units
167 units (165 units - US) and (2 units - International)
Sold at
US Nationwide Distribution to AL, MA, MD, MN, MO, NE, NJ, OK, OR, PA and VA; and Canada
Description
Potential for a leak to occur on the back-up O2 and air e-size cylinder yokes on the A7 Anesthesia Delivery System.
Product
A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. Part numbers 0632F-PA0000X (US domestic) and 0632B-00014 (international)
Manufacturer(s)
Mindray DS USA, Inc. dba Mindray North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →