Device recall
Z-0683-2017: Lineage Liners: REF 70102846, REF 70202852, REF 70202852, REF 70302858, REF…
FDA device recall · Class III · MicroPort Orthopedics Inc.
Key facts
| Recall number (Z-number) | Z-0683-2017 |
|---|---|
| Recall event | 75063 |
| Product | Lineage Liners: REF 70102846, REF 70202852, REF 70202852, REF 70302858, REF 70303258, REF 70402864, REF 70403264, REF 70403664 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