Aesculap Inc: Medical Device Recall in 2024 - (Recall #: Z-1244-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.

Product Classification:

Class II

Date Initiated: January 9, 2024

Date Posted: March 13, 2024

Recall Number: Z-1244-2024

Event ID: 93856

Reason for Recall:

The sterile blister packaging may be damaged, and sterility may be compromised.

Status: Ongoing

Product Quantity: 18 pieces

Code Information:

Product Code: EK230SU; UDI/DI: 04046963620455; Batch Numbers (Expiration Date): 52481826 (02/29/2024), 52644661 (02/28/2026);

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated