Device recall
Z-2588-2016: PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended…
FDA device recall · Class II · MicroPort Orthopedics Inc.
Key facts
| Recall number (Z-number) | Z-2588-2016 |
|---|---|
| Recall event | 74752 |
| Product | PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients. |
| Product code | LWJ |
| Recalling firm | MicroPort Orthopedics Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 21, 2017 |
| 510(k) numbers | K003016 |
| FEI number | 3010536692 |
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