Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AESCULAP MINOP InVent 30 Trocar System Recalled by Aesculap Implant Systems LLC Due to Aesculap Implant Systems LLC is recalling the Minop...
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
AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.
Quantity: 21 units distributed in U.S.
Why Was This Recalled?
Aesculap Implant Systems LLC is recalling the Minop Trocar due to the possibility it may have sharp edges on the distal end which may lead to the abrasion of the insulation when removing the electrode.
Where Was This Sold?
Product was distributed throughout the United States and Canada.
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