Device recall
Z-2314-2012: TxRx Knee 15 Coil 3T. For use in conjunction with magnetic resonance scanners to…
FDA device recall · Class II · Quality Electrodynamics LLC
Key facts
| Recall number (Z-number) | Z-2314-2012 |
|---|---|
| Recall event | 62949 |
| Product | TxRx Knee 15 Coil 3T. For use in conjunction with magnetic resonance scanners to produce diagnostic images of the knee that can be interpreted by a trained physician. |
| Product code | MOS |
| Recalling firm | Quality Electrodynamics LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 19, 2013 |
| 510(k) numbers | K082636 |
| FEI number | 3007350713 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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