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Aesculap Inc recalls DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
Recalled March 13, 2024 · FDA recall Z-1244-2024 · Aesculap
Hazard
The sterile blister packaging may be damaged, and sterility may be compromised. · FDA Class II
Units
18 pieces
Sold at
Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada.
Description
The sterile blister packaging may be damaged, and sterility may be compromised.
Product
DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
Manufacturer(s)
Aesculap Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →