Medartis recalls
4 federal recalls on file, showing the 3 from the last 12 months. We read every CPSC, FDA, USDA and NHTSA notice for Medartis and put it in plain English.
Recent recalls
Medartis APTUS TriLock plate recalled for incorrect bendingMedartis AG recalled one lot of its APTUS TriLock scaphoid bone plate, model A-4350.81, because the plate may be incorrectly bent. The notice reports no injuries. The 65 affected units were distributed nationwide, including in Indiana, Arizona, California, and New York.
ModerateFDANov 12, 2026
- Medartis 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.
ModerateFDAJun 17, 2026
- Check 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.
ModerateFDAMar 18, 20262 products