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Materialise USA LLC recalls ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
Recalled August 31, 2022 · FDA recall Z-1569-2022 · Materialise USA
Hazard
MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK · FDA Class II
Units
1 unit
Sold at
US Nationwide distribution in the state of MD.
Description
MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK
Product
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
Manufacturer(s)
Materialise USA LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →