Brand

Materialise N.v. Recalls

5 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Materialise N.v..

5Total Recalls
0Critical
8Units Affected
Jun 19, 2023Most Recent
All Recalls

Every Materialise N.v. Recall

Sorted by most recent. Click any recall for full details.

5 recalls
High RiskFDA
Materialise N.v.
ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgical instruments in ...
Surgical Devices·1 affected·Jun 19, 2023
High RiskFDA
Materialise N.v.
TRUMATCH Orthognathic - Full Bimaxillary Surgical Kit, Catalog Number SD980.001
Surgical Devices·1 affected·Feb 3, 2020
High RiskFDA
Materialise N.v.
TRUMATCH Orthognathics - Genioplasty Surgical Kit, Add-on, Catalog Number: SD980.013
Surgical Devices·1 affected·Feb 3, 2020
High RiskFDA
Materialise N.v.
Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide during surgical procedure for total and partial ...
Surgical Devices·4 affected·Sep 23, 2015
High RiskFDA
Materialise N.v.
Signature TKA GDE/MDL Set 04-05 (Femur & Tibia) The Signature Patient-Specific Surgical Guides are intended to be used as part of the ...
Surgical Devices·1 affected·Feb 4, 2015