FDAMarch 7, 2017device

AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.

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

The hazard

Aesculap Implant Systems LLC is recalling the Minop Trocar due to the possibility it may have sharp edges on the distal end which may lead to the abrasion of the insulation when removing the electrode.

What to do

FDA enforcement status: Terminated

Brands named

aesculap implant systemsaesculapaesculap implant

Recall history

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

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