FDAMay 28, 2019device

The ICS CHARTR EP 200

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

The hazard

There is a risk to the healthcare professional or patient of exposure to undergrounded electrical surfaces which may result in an electrical shock.

What to do

FDA enforcement status: Terminated

Brands named

gn otometrics

UPCs

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Recall history

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

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