Materialise Usa recalls

Materialise Usa appears in 6 official U.S. recall notices indexed by RecallRadar, most recently on 2022-08-31.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
  FDA Device · Class II · 2022-08-31 · Materialise Usa
• Signature TKA GDE/MDL Set 04-05 Patient-specific surgical guide and instrument set
  FDA Device · Class II · 2016-06-15 · Materialise Usa
• Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Tibia) is intended to be used as a surgical instrument to assist in the…
  FDA Device · Class II · 2014-12-03 · Materialise Usa
• REF 42-411571 QTY 1 CATALOG CAUTION. SEE INSTRUCTIONS FOR USE SIGNATURE M PKA GDE/MDL SET SML-MP DD.....R-FEB55RKA-T JA-A01 05551 PKA POST…
  FDA Device · Class II · 2014-01-15 · Materialise Usa
• ProPlan CMF Guide(s) Model(s) REF SD900.008 Description: Single Use Only : Patient-Specific Guide, Orthognathic, Intermediate Single Use On…
  FDA Device · Class II · 2014-01-01 · Materialise Usa
• ProPlan CMF Guide(s) Model(s) REF SD900.008 Description: Single Use Only : Patient-Specific Guide, Orthognathic, Final Single Use Only Rx o…
  FDA Device · Class II · 2014-01-01 · Materialise Usa