Device recall
Z-2243-2020: Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage…
FDA device recall · Class II · Med Tec Inc
Key facts
| Recall number (Z-number) | Z-2243-2020 |
|---|---|
| Recall event | 85654 |
| Product | Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioning. |
| Product code | IYE |
| Recalling firm | Med Tec Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 25, 2021 |
| 510(k) numbers | K933227 |
| FEI number | 1000143606 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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