Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The sterile blister packaging may be damaged, and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aesculap Inc directly.
Affected Products
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.
Quantity: 6 pieces
Why Was This Recalled?
The sterile blister packaging may be damaged, and sterility may be compromised.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aesculap Inc
Aesculap Inc has 18 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report