FDAMarch 31, 2021device

ELI 380 Electrocardiograph, 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

732094265415118490001284119150000588120090001355120090001354812345026757117120557018117120557019117120557020117120557021117230571942117230571943

Recall history

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

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ELI 380 Electrocardiograph, 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. — Recall Details · AllClear