Recall Z-1485-2026— Aesculap Inc

Name: FDA recall Z-1485-2026
Creator: U.S. Food and Drug Administration
Published: 2026-01-15

Class II · Ongoing

Class II FDA medical device recall by Aesculap Inc, initiated 2026-01-15. It names one FDA 510(k) clearance: K983365. Product: Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A. Reason: There is the potential for the length of the trocar shaft to be too long..

Recalling firm: Aesculap Inc
Classification: Class II
Status: Ongoing
Initiated: 2026-01-15
Firm location: Center Valley, PA, United States

510(k) clearances named in this recall

1 on FDA's record

K983365 — AESCULAP MINOP SYSTEMAesculap, Inc.·cleared 1998-12-18

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.