FDA Recall Terminated

OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

Recall: Z-2040-2012 · Initiated November 20, 2006

Recall

Recall Number
Z-2040-2012
Event Number
62382
Firm
GE OEC Medical Systems, Inc
FEI Number
1720753
Product Code
OXO
Status
Terminated
Root Cause
Device Design
Initiated
November 20, 2006
Posted
July 24, 2012
Terminated
May 13, 2013
Address
384 Wright Brothers Dr, Salt Lake City, UT, 84116-2862

Description

OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

Reason

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. The OEC 6800 Miniview was recalled in November 2006 due to several intermittent potential safety issues including navigation tracking inaccuracy, system Lock-up, incorrect image display, incorrect dose area calculated air kerma in "film mo

Action

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. On 11/20/2006, two written notifications were sent to 1513 identified consignees, addressed to the Facility Administrator and the Radiology Administrator for a combined total of 3026 letters. The Urgent Recall Notice, dated 11/8/2006, advised customers that GE Healthcare had identified several intermittent potential safety issues that may occur with the identified affected product. The notification also provided interim or permanent solutions for each of the problems described. For the issues that did not have permanent solutions at the time, the firm was to contact customers and remedy the issues free of charge. For the issues that did have a permanent fix at the time, the GEHC OEC service team was to contact customers to install the correction. If customers had questions or concerns, they were to contact the service team for further information at 800-874-7378 option 8. On 04/23, 2007, a second written notification was sent via certified mail to the same 1513 consignees providing further clarification on the issue of "incorrect Image Display" and a temporary remedy to the issue.

Distribution

Worldwide Distribution

Quantity

1,933 units