Device recall
Z-0686-2017: Lineage Shell: REF 36693646, REF 36693848, REF 36694050, REF 36694252, REF…
FDA device recall · Class III · MicroPort Orthopedics Inc.
Key facts
| Recall number (Z-number) | Z-0686-2017 |
|---|---|
| Recall event | 75063 |
| Product | Lineage Shell: REF 36693646, REF 36693848, REF 36694050, REF 36694252, REF 36694454, REF 36694656, REF 36694858, REF 36695060, REF 36695262, REF 36695464 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