FDANovember 16, 2020device

Capnostream 35 Portable Respiratory Monitor, Product numbers PM35MN02, PM35MN01, PM35MN05, DLPM35MN02 - Product Usage: use during both no motion and motion conditions and for patients who are well or poorly perfused.

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

The hazard

The firm has released software update V01.05.02.16 (also known as V1.5.2) in response to customer reports of a false display of the message, "Temperature Exceeds Limits" followed by automatic shutdown of the monitor with no accompanying alarm.

What to do

FDA enforcement status: Ongoing

Brands named

covidien

Recall history

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

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