FDAJanuary 4, 2022device

The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten alloy attached to a proximal stainless steel hypo-tube and distal body coil delivery pusher with a radiopaque distal positioning marker and proximal fluorosafe marker. The Optima Coil delivery pus...

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

The hazard

Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf carton label or pouch label due to inadequate manufacturing line clearance. As a result of this labeling mix-up, there is the possibility of inadvertently selecting the incorrect coil size for the procedure potentially causing some harms like vessel damage, an inability to treat with said device and potential rupture of the aneurysm.

What to do

FDA enforcement status: Ongoing

Brands named

balt

UPCs

0081805302601000818053026096

Recall history

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

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