Device recall
Z-2059-2013: Philips Easy Upgrade DR, Code No: 712086 This system is used for making X-Ray…
FDA device recall · Class II · Philips Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-2059-2013 |
|---|---|
| Recall event | 65950 |
| Product | Philips Easy Upgrade DR, Code No: 712086 This system is used for making X-Ray exposures for diagnostics. |
| Product code | KPR |
| Recalling firm | Philips Healthcare Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 3, 2020 |
| 510(k) numbers | K982795 |
| FEI number | 1218950 |
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