FDAMarch 31, 2021device

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

812345029666119030001449119030001451119030001447119030001450119190000644117200568671116520545406118030607566117510602011117060553537118030607568

Recall history

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

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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. — Recall Details · AllClear