Device recall
Z-0699-2025: EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR…
FDA device recall · Class II · MicroPort Orthopedics Inc.
Key facts
| Recall number (Z-number) | Z-0699-2025 |
|---|---|
| Recall event | 95672 |
| Product | EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE 6 LEFT PRIMARY, REF: EFSRN6PL Knee prosthesis component |
| Product code | MBH |
| Recalling firm | MicroPort Orthopedics Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K093552, K102380 |
| 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