FDAOctober 5, 2017device

MONTERIS MEDICAL NEUROBLATE SYSTEM, used for MRI-guided neurosurgical ablation.

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

The hazard

The firm received complaints that involved an unanticipated interaction between a NeuroBlate system and 1.5 Tesla (1.ST) MRI systems.

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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