FDAJanuary 11, 2024device

The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the infusion of the Onyx liquid embolic system (LES). The catheter has a semi-rigid proximal shaft and a highly flexible distal shaft to facilitate the advancement of the catheter in t...

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

The hazard

European version of microcatheter were distributed within US which contain a different "Indications for Use".

What to do

FDA enforcement status: Ongoing

Brands named

micro therapeuticsmicro

UPCs

00763000311445

Recall history

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

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The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the infusion of the Onyx liquid embolic system (LES). The catheter has a semi-rigid proximal shaft and a highly flexible distal shaft to facilitate the advancement of the catheter in t... — Recall Details · AllClear