FDAFebruary 26, 2018device

MindFrame Capture LP Revascularization Devices: Product Numbers: (a) REF 300010 (b) REF 300011 (c) REF 300012 (d) REF 300013 (e) REF 300014 (f) REF 300015 (g) REF 300016 (h) REF 300017 (i) REF 300018 Intended to restore blood flow by removing thrombus from a large intracranial vessel experiencing...

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

The hazard

There is a potential issue for all MindFrame Capture devices to partially detach or separate from the delivery wire.

What to do

FDA enforcement status: Terminated

Brands named

micro therapeutics inc dba ev3 neurovascularmicromicro therapeutics

UPCs

008438890313340084388903134100847536020207008438890313650084388903137200847536020214008438890313960084388903140200847536020221008438890314260084388903143300847536020238

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →