Every recall we track for Materialise N.V. — 5 in all — plus the complaints and injury reports the public filed about them.
Materialise recalls ProPlan CMF Patient-Specific Mandible Guides 3A and : Wrong versions shipped before redesign request. Check identification number SD900.101 or UDI 05420060351013.
Materialise recalls MRI Biomet Pin Guides for Total Knee Arthroplasty due to risk of wrong tibia guide being included for different patient cases. Affected patients should contact for remedy.
Materialise recalls Match Point System surgical instruments due to incorrect procedure side labeling in Shoulder Case Planning Reports, which could lead to surgical errors.
Materialise recalls TRUMATCH Orthognathics Genioplasty Surgical Kit add-on (SD980.013) due to plate mismatch with package labeling. Affected units may have incorrect surgical components.
Materialise recalls TRUMATCH Orthognathic Full Bimaxillary Surgical Kit (SD980.001) due to custom surgical plate not matching package labeling. Affected units may have incorrect plate design.
