Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DS Titanium Ligation Clip Recalled by Aesculap Implant Systems LLC Due to Added a contraindication to IFU: Do not use...
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 Implant Systems LLC directly.
Affected Products
DS Titanium Ligation Clip, used in laparoscopic surgery
Quantity: 9621
Why Was This Recalled?
Added a contraindication to IFU: Do not use the DS clips for living donor nephrectomies. Added other contraindications. A publication from 2017 recommended Aesculap DS Clips for kidney transplantation with living donors. The information from this publication was not approved or validated by the firm.
Where Was This Sold?
US and Canada distribution
About Aesculap Implant Systems LLC
Aesculap Implant Systems LLC has 61 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report