FDA-Device2017-04-19Class II
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.
Aesculap Implant Systems LLC
Hazard
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.
Sold states
Product was distributed throughout the United States and Canada.
Affected count
21 units distributed in U.S.
Manufactured in
3773 Corporate Pkwy, N/A, Center Valley, PA, United States
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.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1814-2017Don't want to check this manually?
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