Device recall
Z-0522-04: Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device
FDA device recall · Class III · Siemens Medical Solutions USA, Inc
Key facts
| Recall number (Z-number) | Z-0522-04 |
|---|---|
| Recall event | 28046 |
| Product | Magnetom Allegra System. Nuclear Magnetic Resonance Imaging Diagnostic Device |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 9, 2004 |
| 510(k) numbers | K002179 |
| FEI number | 2240869 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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