Device recall
Z-2858-2018: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
FDA device recall · Class II · Philips Medical Systems Gmbh, DMC
Key facts
| Recall number (Z-number) | Z-2858-2018 |
|---|---|
| Recall event | 80577 |
| Product | DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 |
| Product code | MQB |
| Recalling firm | Philips Medical Systems Gmbh, DMC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 30, 2024 |
| 510(k) numbers | K090625 |
| FEI number | 3003768251 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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