Device recall
Z-0684-2017: Dynasty Liners: REF DLCOGA28, REF DLCOGB32, REF DLCOGC36, REF DLCOGD38, REF…
FDA device recall · Class III · MicroPort Orthopedics Inc.
Key facts
| Recall number (Z-number) | Z-0684-2017 |
|---|---|
| Recall event | 75063 |
| Product | Dynasty Liners: REF DLCOGA28, REF DLCOGB32, REF DLCOGC36, REF DLCOGD38, REF DLCOGE40, REF DLCOGF42, REF DLCOGG44, REF DLCOGH48, REF DLCOGJ52, REF DLCOGK56, For use with the conserve metal head |
| Product code | LZO |
| Recalling firm | MicroPort Orthopedics Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 1, 2017 |
| 510(k) numbers | K100866 |
| FEI number | 3010536692 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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