FDANovember 24, 2019device

Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System, REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, and MV-A...

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

The hazard

The devices may be missing the implant coil.

What to do

FDA enforcement status: Terminated

Brands named

microvention

Recall history

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

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