FDAMarch 31, 2021device

Surveyor S12/S19 Bedside Patient Monitor, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version 1.5.1 - Product Usage: indicated for use on adult and pediatric populations.

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

The hazard

Devices do not meet IEC 60601-2-27 requirements as labeled.

What to do

FDA enforcement status: Terminated

Brands named

welch allyn inc mortarawelchwelch allyn

UPCs

732094288926118300000441118300000440118300000438118300000439118350000999118350000998118350000997118350000996119100001366119100001369119100001367

Recall history

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

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