Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DS Titanium Ligation Clip Appliers 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 Appliers, used in laparoscopic surgery
Quantity: 270
Why Was This Recalled?
Added a contraindication to IFU: Do not use the DS clips for living donor nephrectomies. Added other contraindications. Updated cleaning and sterilization instructions.
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