Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Gomco Circumcision Clamps with separate O-Ring Component: The device is Recalled by Aesculap Implant Systems LLC Due to Aesculap has received complaints of excessive bleeding after...
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
Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life The Gomco clamp is intended to be used for circumcision surgeries
Quantity: 437 units
Why Was This Recalled?
Aesculap has received complaints of excessive bleeding after use of Gomco Circumcision Clamps.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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