Materialise N.V. recalls

7 recalls on record · latest: June 19, 2023

Official U.S. recall history for Materialise N.V., compiled from official government records.

Get recall alerts

Free email alert whenever Materialise N.V. has a new recall — straight from official government data. Unsubscribe anytime.

Materialise N.V. recalls ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgic…

June 19, 2023 · Medical device recalls Moderate risk Wrong versions of guides 3A and 3B (Patient Specific) were shipped prior to the…

Materialise N.V. recalls MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched de…

April 26, 2023 · Medical device recalls Moderate risk The wrong tibia guide was included intended for a different patient case.

Materialise N.V. recalls Match Point System The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperati…

July 17, 2020 · Medical device recalls Moderate risk The procedure side indicated in the top header of the Shoulder Case Planning Re…

Materialise N.V. recalls TRUMATCH Orthognathic - Full Bimaxillary Surgical Kit, Catalog Number SD980.001

February 3, 2020 · Medical device recalls Moderate risk Custom surgical kits contain a plate different than indicated by the package la…

Materialise N.V. recalls TRUMATCH Orthognathics - Genioplasty Surgical Kit, Add-on, Catalog Number: SD980.013

February 3, 2020 · Medical device recalls Moderate risk Custom surgical kits contain a plate different than indicated by the package la…

Materialise N.V. recalls Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide during surgical procedure for…

September 23, 2015 · Medical device recalls Moderate risk Potential inaccuracies in the alignment of the guides. Surgery was inaccurately…

Materialise N.V. recalls Signature TKA GDE/MDL Set 04-05 (Femur & Tibia) The Signature Patient-Specific Surgical Guides are intended to be used…

February 4, 2015 · Medical device recalls Moderate risk Images belonging to a different patient were used for the production of the pat…