| Nombre | Clasificación | Fabricante | Nivel de riesgo | País | Fuente |
|---|---|---|---|---|---|
| Device Recall SYSTEM 1E liquid chemical sterilant processing system | General Hospital and Personal Use Devices | Steris Corporation Hopkins Facility | 2 | United States | USFDA |
| Steris Quick Connects (QC) QFC1728 and QFC1729 | General Hospital and Personal Use Devices | Steris Corporation Hopkins Facility | 2 | United States | USFDA |