Device recall
Z-0794-2019: Ascension Modular Radial Head (MRH) Radial Head Implant, Catalog Number…
FDA device recall · Class III · Ascension Orthopedics, Inc
Key facts
| Recall number (Z-number) | Z-0794-2019 |
|---|---|
| Recall event | 81782 |
| Product | Ascension Modular Radial Head (MRH) Radial Head Implant, Catalog Number, MRH-350-04-WW |
| Product code | HSD |
| Recalling firm | Ascension Orthopedics, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 22, 2019 |
| 510(k) numbers | K062861 |
| FEI number | 3002788818 |
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