| Nombre | Clasificación | Fabricante | Nivel de riesgo | País | Fuente |
|---|---|---|---|---|---|
| Device Recall R3 Forte Ceramic Liners | Orthopedic Devices | Smith & Nephew Inc | 3 | United States | USFDA |
| Device Recall R3 Forte Ceramic Liners | Orthopedic Devices | Smith & Nephew Inc | 3 | United States | USFDA |
| GENESIS(R) II, NONPOROUS TIBIAL BASE, SIZE 5, LEFT | Orthopedic Devices | Smith & Nephew Inc | 2 | United States | USFDA |
| GENESIS(R) II, NONPOROUS TIBIAL BASE, SIZE 6, RIGHT | Orthopedic Devices | Smith & Nephew Inc | 2 | United States | USFDA |
| Smith & Nephew PERILOC VOLAR DISTAL RADIUS PLATE STANDARD 3 HOLE | Orthopedic Devices | Smith & Nephew, Inc. | 2 | United States | USFDA |
| PERILOC Volar Distal Radius 3 Hole Plate | Orthopedic Devices | Smith & Nephew, Inc. | 2 | United States | USFDA |
| LEGION LWEDGE | Orthopedic Devices | Smith & Nephew, Inc. | 2 | United States | USFDA |
| TRIGEN INTERTAN 10S | Orthopedic Devices | Smith & Nephew, Inc. | 2 | United States | USFDA |