Skip to main content
Recall Canary
Aesculap Minop Trocar
← Back to all recalls
MEDICAL DEVICE RECALLMODERATE

Aesculap Minop Trocar

Aesculap is recalling the Minop Trocar 150mm because the shaft may be too long.

What to do

Stop using the affected device and contact Aesculap for further instructions regarding return or replacement.

Recalled
Listed
Updated
Recall No.
Z-1485-2026
Agency
FDA
Firm
Aesculap Inc
Recall ID
98301
Status
ONGOING

Recall at a glance

Quantity recalled
126 units

Why it was recalled

Aesculap is recalling the Minop Trocar 150mm due to a manufacturing defect where the trocar shaft may be too long. This issue was distributed nationwide.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

AESCULAP MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM

UDI-DI
04038653065547
Model/Catalog number
FF399R

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

← Back to all recalls

Editorial summary by Recall Canary · summary updated 2026-06-11 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification