Recall Z-1476-04 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
Siemens Medical Solutions USA, Inc
Siregraph CF X-Ray System. Fluoroscopic image intensified. Model number 4466041
| Date | Sep 18, 2004 (initiated Jun 7, 2004) |
| Status | Terminated |
| Reason | X-ray tube movement when table is tilted more than 90 degrees |
| Root cause | Other |
| Action | The recalling firm issued a Customer DAfety Advisory letter dated 6/7/04 to the hospitals. The letter informs them of the potential problem and provides preventative measures to avoid its occurance. |
| Quantity | 1 unit |
| Distribution | The products were shipped to medical facilities in FL, IL, MI, NH, NJ, PA, and TX. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K960266 | SIREGRAPH CF Siemens Medical Solutions USA, Inc., Mar 11, 1996 |