Aesculap Implant Systems LLC: Medical Device Recall in 2017 - (Recall #: Z-1814-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: March 7, 2017

Date Posted: April 19, 2017

Recall Number: Z-1814-2017

Event ID: 76769

Reason for Recall:

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.

Status: Terminated

Product Quantity: 21 units distributed in U.S.

Code Information:

Item # FH620R

Distribution Pattern:

Product was distributed throughout the United States and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated