Materialise Usa Llc
Plymouth, MI
This page shows every FDA and USDA recall linked to Materialise Usa Llc. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
8
Total Recalls
2012
First Recall
2022
Most Recent
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear
Identification number SD900.208
Jul 13, 2022
· Device
Completed
Signature TKA GDE/MDL Set 04-05
Patient-specific surgical guide and instrument set.
May 3, 2016
· Device
Terminated
Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Tibia) is intended to be used as a surgica...
Nov 21, 2014
· Device
Terminated
REF 42-411571 QTY 1 CATALOG CAUTION. SEE INSTRUCTIONS FOR USE
SIGNATURE
M PKA GDE/MDL SET SML-MP
DD.....R-FE...
Jan 3, 2014
· Device
Terminated
ProPlan CMF Guide(s) Model(s)
REF SD900.008 Description: Single Use Only : Patient-Specific Guide, Orthognat...
Dec 26, 2013
· Device
Terminated
ProPlan CMF Guide(s) Model(s)
REF SD900.008 Description: Single Use Only : Patient-Specific Guide, Orthognat...
Dec 26, 2013
· Device
Terminated
PATIENT SPECIFIC INSTRUMENTS
N-K FLEX PIN GUIDES (FEMUR AND TIBIA)
NONSTERILE ~ MUST BE STERILIZED PRIOR TO US...
May 14, 2012
· Device
Terminated
PATIENT SPECIFIC INSTRUMENTS
LPS-FLEX PIN GUIDES (FEMUR AND TIBIA)
NONSTERILE ~ MUST BE STERILIZED PRIOR TO US...
May 14, 2012
· Device
Terminated