Device recall
Z-1569-2022: ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number…
FDA device recall · Class II · Materialise USA LLC
Key facts
| Recall number (Z-number) | Z-1569-2022 |
|---|---|
| Recall event | 90704 |
| Product | ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208 |
| Product code | HWT |
| Recalling firm | Materialise USA LLC |
| Recall class | Class II |
| Status | Completed |
| FEI number | 3005718816 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database