FDA Device recall Z-1569-2022
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
- FDA Device
- Class II
- completed
- Published 2022-08-31
On 2022-08-31 the FDA classified a Class II recall of ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208 by Materialise Usa, citing MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1569-2022 |
| Classification | Class II |
| Status | completed |
| Initiated | 2022-07-13 |
| Published | 2022-08-31 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Materialise Usa |
| Distribution | US |
Product
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
Reason
MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK
Identifiers
| code_info | Unique Device Identifier (01)05420060352089(10)MU22INADUQ Lot Number: MU22-INQ-DUQ |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1569-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.