FDAMarch 25, 2016device

NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe, Sterile EO. Model #s SFS000-01,SFS002-01, SFS122-01, SFS222-01, SFS322-01, SFS422-01, and SFS522-01. NeuroBlate System SideFire Select Directional Laser Probes are part of the NeuroBlate System. The Monteris Medical NeuroBlate Syst...

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

The hazard

Monteris received a report that the sapphire lens on a 2.2SF probe fractured during a LITT procedure, with resulting introduction of C02 into the patient's brain.

What to do

FDA enforcement status: Terminated

Brands named

monteris medicalmonteris

Recall history

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

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