Device recall
Z-0687-2017: Conserve Shells: REF 38021146, REF 38021148, REF 38021150, REF 38021152, REF…
FDA device recall · Class III · MicroPort Orthopedics Inc.
Key facts
| Recall number (Z-number) | Z-0687-2017 |
|---|---|
| Recall event | 75063 |
| Product | Conserve Shells: REF 38021146, REF 38021148, REF 38021150, REF 38021152, REF 38021154, REF 38021156, REF 38021158, REF 38021160, REF 38021162, REF 38021164, REF 38023642, REF 38023646, REF 38023844, REF 38023848, REF 38024046, REF 38024050, REF 38024248, REF 38024252, REF 38024450, REF 38024454, REF… |
| 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