FDAAugust 14, 2018device

APTIO RACK INPUT MODULE

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

The hazard

The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.

What to do

FDA enforcement status: Terminated

Brands named

siemens healthcare diagnosticssiemenssiemens healthcare

UPCs

00630414594477

Recall history

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

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