Plymouth, MI, United States
Materialise USA LLC recalls
1 recall recorded since 2018, most recently on 13 July 2022. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Completed Class II Medical devices
- Recall started
- 13 July 2022
- Reason
- MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK
- Distribution
- US Nationwide distribution in the state of MD.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1569-2022
- ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.