Date Initiated by Firm |
March 01, 2007 |
Date Posted |
September 28, 2007 |
Recall Status1 |
Terminated 3 on May 01, 2012 |
Recall Number |
Z-0677-2007 |
Recall Event ID |
37498 |
510(K)Number |
K024012 K022069 K021049
|
Product Classification |
Image-intensified fluoroscopic x-ray system - Product Code JAA
|
Product |
OEC 9800 image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. |
Code Information |
Serial Numbers: 429 units within the range 8S-0007 thru 8S-7163, 455 units within the range 89-0014 thru 89-3520, 659 units within the range 82-0010 thru 82-7138. |
Recalling Firm/ Manufacturer |
GE OEC Medical Systems, Inc 384 Wright Brothers Dr Salt Lake City UT 84116-2862
|
For Additional Information Contact |
Karen Tolson 847-501-1884
|
Manufacturer Reason for Recall |
During routine service, primary and/or secondary collimators may not have been properly reinstalled.
|
FDA Determined Cause 2 |
Other |
Action |
Customers were notified by letter on 03/01/2007. They were told to continue using the machines and that an inspection would be scheduled immediately to verify that collimators had been correctly installed. |
Quantity in Commerce |
1857 units |
Distribution |
Nationwide and Germany. |
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 = JAA and Original Applicant = GE OEC MEDICAL SYSTEMS
|