FDAMarch 1, 2018device

Fabius GS Premium, anesthesia machine, catalog no. 8607000 Product Usage: The products are inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders. Fa...

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

The hazard

The automatic ventilation may fail if the position detection of the motor is disturbed. If the ventilator cover is damaged, manual ventilation may also fail.

What to do

FDA enforcement status: Terminated

Brands named

draeger medicaldraeger

Recall history

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

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Fabius GS Premium, anesthesia machine, catalog no. 8607000 Product Usage: The products are inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders. Fa... — Recall Details · AllClear