Device recall
Z-1561-2016: Radionuclide Radiation Therapy System Product The product is a teletherapy…
FDA device recall · Class II · Elekta, Inc.
Key facts
| Recall number (Z-number) | Z-1561-2016 |
|---|---|
| Recall event | 73761 |
| Product | Radionuclide Radiation Therapy System Product The product is a teletherapy device intended for stereotactic irradiation of head structures ranging from very small target sizes of a few millimeters to several centimeters. |
| Product code | IWB |
| Recalling firm | Elekta, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 16, 2021 |
| 510(k) numbers | K151159, K151561 |
| FEI number | 1037831 |
At a glance
- 1–9 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