| Nombre | Clasificación | Fabricante | Nivel de riesgo | País | Fuente |
|---|---|---|---|---|---|
| Device Recall STERIS 4805 | General and Plastic Surgery Devices | Steris Corporation | 1 | United States | USFDA |
| Device Recall Reliance 1227 | General Hospital and Personal Use Devices | Steris Corporation | 2 | United States | USFDA |
| STERIS 5085 and 5085SRT surgical tables | General and Plastic Surgery Devices | Steris Corporation | 1 | United States | USFDA |
| AMSCO Evolution steam sterilizer Transfer Carriage | General Hospital and Personal Use Devices | Steris Corporation | 2 | United States | USFDA |
| VERIFY Dual Species SelfContained Biological Indicator | General Hospital and Personal Use Devices | Steris Corporation | 2 | United States | USFDA |
| STERIS 5085 and 5085SRT Surgical Table | General and Plastic Surgery Devices | Steris Corporation | 1 | United States | USFDA |
| AMSCO | General Hospital and Personal Use Devices | Steris Corporation | 2 | United States | USFDA |
| Harmony Insight Diagnostic Monitor Support System | General and Plastic Surgery Devices | Steris Corporation | 2 | United States | USFDA |