Recall Z-0009-04 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
Siemens Medical Solutions USA, Inc
Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive
| Date | Oct 15, 2003 (initiated Aug 8, 2003) |
| Status | Terminated |
| Reason | possible movement of table tilt and table longitudinal |
| Root cause | Other |
| Action | The recalling firm issued Update Instructions SP016/03/S, SP017/03S and SP018/03/S that instruct the Service Engineers to visit each affected system to install the required parts. |
| Quantity | 34 units |
| Distribution | Nationwide. The product was shipped to medical facilities in CA, FL, GA, IL, MD, NC, NJ, NY, OK, PA, SC, TN, TX, VA, WI, and WV. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K923049 | UROSKOP D1, UROSKOP D2, AND UROSKOP D3 Siemens Medical Solutions USA, Inc., Sep 15, 1992 |