Official recall notice
FDA DeviceClass IINotable
FDA Recall: Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: F
- Recall date
- 2026-03-11
- Brand
- Aesculap Inc
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
There is the potential for the length of the trocar shaft to be too long.
Recommended action
What to do
126 units
Product description
There is the potential for the length of the trocar shaft to be too long.