Device recall
Z-2743-2015: PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree…
FDA device recall · Class I · MicroPort Orthopedics, Inc.
Key facts
| Recall number (Z-number) | Z-2743-2015 |
|---|---|
| Recall event | 71925 |
| Product | PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper. Orthopedic hip prosthesis component. |
| Product code | MBL |
| Recalling firm | MicroPort Orthopedics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 17, 2018 |
| 510(k) numbers | K091423, K100866 |
| 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