FDAMarch 15, 2016device

GE Healthcare, Aisys and Aisys CS2. Intended to provide general inhalation anesthesia and ventilator support to a wide range of patients (neonatal, pediatric, and adult).

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The vacuum suction tubing could be kinked within the machine resulting in suction less than the 20 lpm required by ISO 10079-3. This could result in inadequate suction performance to clear the airway and inadequate ventilation of the patient.

What to do

FDA enforcement status: Terminated

Brands named

ge medical systems

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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