Device recall
Z-0479-2022: Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version…
FDA device recall · Class II · PTW NORTH AMERICA CORPORATION
Key facts
| Recall number (Z-number) | Z-0479-2022 |
|---|---|
| Recall event | 89314 |
| Product | Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032 |
| Product code | IYE |
| Recalling firm | PTW NORTH AMERICA CORPORATION |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 9, 2024 |
| 510(k) numbers | K160405 |
| FEI number | 3019665367 |
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