GE Healthcare recalls GE Healthcare, Aespire 7900, Aespire View Anesthesia Machines. Model numbers 1009-9012-000. Intended to provide gene

Recalled April 8, 2015 · FDA recall Z-1376-2015 · GE Healthcare

Hazard

Specific Aespire 7900 Anesthesia Machines have an increased likelihood of failure of the CPU circuit board. This could result in a blank display or loss of mechanical ventilation. · FDA Class II

Units

46 (10 units US, 36 units OUS)

Sold at

Worldwide Distribution -- US, including the states of NC and OK; and the countries of CHINA, INDIA, JAPAN, MEXICO, and VENEZUELA.

Description

Specific Aespire 7900 Anesthesia Machines have an increased likelihood of failure of the CPU circuit board. This could result in a blank display or loss of mechanical ventilation.

Product

GE Healthcare, Aespire 7900, Aespire View Anesthesia Machines. Model numbers 1009-9012-000. Intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients

Manufacturer(s)

GE Healthcare

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →