OEC 9900 Elite Fluoroscopy System, Catalog No. 887208 and 887210, GE OEC Medical Systems, Inc.
FDA device recall Z-0042-2007 · posted 2006-10-14 · Terminated
Recall details
- Recalling firm
- GE OEC Medical Systems, Inc
- Reason for recall
- X-ray system may lose or mix images and/or lose patient data.
- Action taken
- Consignees will be notified by letter beginning 10/21/2006.
- Root cause
- Other
- Status
- Terminated
- Product code
- JAA
- Quantity affected
- 822 units
- Distribution
- Nationwide, including VA facilities in FL, NC, WA and military accounts in GA and WA. Foreign distribution to Australia, Belgium, Canada, Finland, France, Germany, Italy, Netherlands, New Zealand, Sin
- Date initiated
- 2006-09-30
- Date posted
- 2006-10-14
- Date terminated
- 2012-04-16
- Location
- Salt Lake City, UT
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| OEC OLYMPUS MOBILE FLUOROSCOPY SYSTEM WITH INTEGRATED NAVIGATION (K041931) | Ge Oec Medical Systems, Inc. | 2004-08-26 |