FDA-Device2024-03-13Class II
DISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic procedures.
Aesculap Inc
Hazard
The sterile blister packaging may be damaged, and sterility may be compromised.
Sold states
Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada.
Affected count
12 pieces
Manufactured in
3773 Corporate Pkwy, Center Valley, PA, United States
Products
DISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic procedures.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1243-2024Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief