Device recall
Z-0584-2017: RF MultiGen, 0406-900-000; Refurb RF MultiGen, 0406-900-000U
FDA device recall · Class III · Stryker Instruments Div. of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0584-2017 |
|---|---|
| Recall event | 75485 |
| Product | RF MultiGen, 0406-900-000; Refurb RF MultiGen, 0406-900-000U |
| Product code | GXD |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 25, 2017 |
| 510(k) numbers | K071482 |
| FEI number | 1811755 |
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