Device recall
Z-0905-2011: BuckyDiagnost general purpose x-ray system with Optimus Generator. General…
FDA device recall · Class II · Philips Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-0905-2011 |
|---|---|
| Recall event | 58077 |
| Product | BuckyDiagnost general purpose x-ray system with Optimus Generator. General Purpose Diagnostic Radiography. |
| Product code | IZO |
| Recalling firm | Philips Healthcare Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 11, 2020 |
| 510(k) numbers | K9455278 |
| FEI number | 1218950 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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