Class II

Medical Device Recall: DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic procedures.

Aesculap Inc · January 9, 2024

Reason for Recall

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

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

6 pieces

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1246-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.