FDAApril 27, 2022device

AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;

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

The hazard

Due to incorrect size and configuration labeling of the detachable coil system.

What to do

FDA enforcement status: Ongoing

Brands named

micro therapeuticsmicro

UPCs

0084753602959000847536030138

Recall history

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

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