Medartis
4 federal recalls on file, showing the 3 from the last 12 months. We monitor every CPSC, FDA, USDA, and NHTSA notice for Medartis and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-06-17FDA-DeviceClass IIMedartis APTUS compression screws recalled for misaligned hole
Medartis has recalled certain APTUS 5.0 headed cannulated compression screws (CCS) used in bone fixation surgery because the central hole in the screw is not properly centered. This affects 13 units across five states. No injuries have been reported.
- 2026-03-18FDA-DeviceClass IICheck Medartis APTUS screw lot 25467933
Medartis discovered that certain packages labeled as 2.8mm APTUS TriLock Screws may actually contain 2.5mm screws instead. This size mix-up could affect surgical fixation in hand, forearm, shoulder, or foot procedures. The issue affects 126 units distributed in the US (Indiana and Pennsylvania) and 12 European and other countries.
- 2026-03-18FDA-DeviceClass IICheck Medartis APTUS screw lot 25472432
Medartis AG recalled specific lots of APTUS 2.5 TriLock Screws used in hand, forearm, shoulder, and foot surgery because some packages may contain 2.8mm screws instead of the labeled 2.5mm size. Using the wrong size screw could affect surgical fixation.
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