FDASeptember 8, 2023device

F2-01 Frame, physiological patient monitor (with arrhythmia detection or alarms)

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

The hazard

There is a potential interruption of data communication between E-modules inserted in the F2-01 Frame and CARESCAPE ONE and CARESCAPE Canvas 1000 patient monitors if the F2-01 Frame has not been powered down within the last 120 days.

What to do

FDA enforcement status: Ongoing

Brands named

ge medical systems china

Recall history

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

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