← Back to recalls
FDA DeviceClass IINotable

FDA Recall: Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: F

Date: 2026-03-11
Brand: Aesculap Inc
Category: Medical Device
FDA Class: Class II

Description

There is the potential for the length of the trocar shaft to be too long.

Hazard

There is the potential for the length of the trocar shaft to be too long.

Remedy

126 units

View original recall →