FDAAugust 4, 2016device

MISAGO RX Self Expanding Peripheral Stem

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

The hazard

During recent routine testing, the MISAGO Peripheral Stent was found not to conform to product specification related to stent diameter at the proximal/distal ends and/or the shape of the stent.

What to do

FDA enforcement status: Terminated

Brands named

terumo medicalterumo

Recall history

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

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