FDANovember 24, 2019device

Terumo AZUR Peripheral Coil System, Detachable 18, Helical HydroCoil Embolization System, REF numbers 45-481015, 45-481020, 45-481215, 45-481220, 45-481515, 45-481520, 45-482020, 45-482030, 45-480202, 45-480204, 45-480310, 45-480302, 45-480305, 45-480410, 45-480415, 45-480420, 45-480405, 45-48061...

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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Terumo AZUR Peripheral Coil System, Detachable 18, Helical HydroCoil Embolization System, REF numbers 45-481015, 45-481020, 45-481215, 45-481220, 45-481515, 45-481520, 45-482020, 45-482030, 45-480202, 45-480204, 45-480310, 45-480302, 45-480305, 45-480410, 45-480415, 45-480420, 45-480405, 45-48061... — Recall Details · AllClear