Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PRESTIGE RETRACTION GRASPER Recalled by Aesculap Implant Systems LLC Due to Endoscopic graspers may become separated at the weld...
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
PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8361-10
Quantity: 399
Why Was This Recalled?
Endoscopic graspers may become separated at the weld from handle to the shaft of the device.
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