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FDAOctober 22, 2014device

Philips Expression MR200 MRI Patient Monitoring System.

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

The hazard

The MR 200 devices failed the initial power up test due to capacitor short and hi-pot testing; possible loss of Patient Monitoring or User/Service Electrical Shock.

What to do

FDA enforcement status: Terminated

Brands named

invivo

Recall history

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

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