Aesculap Inc: Medical Device Recall in 2024 - (Recall #: Z-1245-2024)

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.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.

Product Classification:

Class II

Date Initiated: January 9, 2024

Date Posted: March 13, 2024

Recall Number: Z-1245-2024

Event ID: 93856

Reason for Recall:

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

Status: Ongoing

Product Quantity: 6 pieces

Code Information:

Product Code: EK234SU; UDI/DI: 04046963620462; Batch Numbers (Expiration Date): 52573073 (12/08/2023);

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated