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MEDICAL DEVICE RECALLMODERATE
Aesculap Minop Trocar
Aesculap is recalling the Minop Trocar 150mm (Model FF399R) due to a potential defect where the trocar shaft length may be too long.
What to do
Stop using the affected trocar and contact Aesculap for further instructions regarding the return or replacement of the device.
Why it was recalled
There is the potential for the length of the trocar shaft to be too long.
How to identify it
UPC 04038653065547
Brand Name: AESCULAP
Where it was sold
Distributed nationwide.
Official source
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Editorial summary by Recall Canary · last updated 2026-06-04 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification