FDASeptember 29, 2016device

Aptio Automation Modules

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

The hazard

Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.

What to do

FDA enforcement status: Terminated

Brands named

siemens healthcare diagnosticssiemenssiemens healthcare

Recall history

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

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