FDAJanuary 9, 2024device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

aesculap

UPCs

04046963620462

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures. — Recall Details · AllClear