| Date Initiated by Firm | December 30, 2004 |
| Date Posted | February 14, 2006 |
| Recall Status1 |
Terminated 3 on February 21, 2006 |
| Recall Number | Z-0219-05 |
| Recall Event ID |
30761 |
| 510(K)Number | K993090 |
| Product Classification |
System, X-Ray, Stationary - Product Code KPR
|
| Product | Proteus XR/a Radiographic X-ray System, models 2259973-1, 2259973-2, 2259973-3, 2259973-4. The system consists of a radiographic table, a overhead tube suspension, high frequency generator and power distribution unit, wall stand, dual focal spot x-ray tube and operator''s console. |
| Code Information |
all serial numbers |
Recalling Firm/ Manufacturer |
General Electric Med Systems LLC 3000 N Grandview Blvd Waukesha WI 53188-1615
|
| For Additional Information Contact | Larry Kroger, Ph.D 262-544-3894 |
Manufacturer Reason for Recall | Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur. |
FDA Determined Cause 2 | Other |
| Action | An 'Urgent: Radiation Safety Notice' letter was issued to hospitals with affected systems describing potential hazards, the planned modification and recommended action to limit the hazard until the planned modification is installed. A GE field Service Representative will install the modification. |
| Quantity in Commerce | 2716 |
| Distribution | globally |
| Total Product Life Cycle | TPLC Device Report |
|
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
|
| 510(K) Database | 510(K)s with Product Code = KPR
|