Toshiba Infinix-i, INFX-8000F The expected usage of these devices is for fluoroscopy studies for various anatomical regions of the human body.
Recall
- Recall Number
- Z-1872-2011
- Event Number
- 58134
- Firm
- Toshiba American Medical Systems Inc
- FEI Number
- 2020563
- Product Code
- JAA
- Status
- Terminated
- Root Cause
- Radiation Control for Health and Safety Act
- Initiated
- December 21, 2010
- Posted
- April 15, 2011
- Terminated
- March 18, 2013
- Address
- 2441 Michelle Dr P.O. Box 2068, Tustin, CA, 92781-2068
Description
Toshiba Infinix-i, INFX-8000F The expected usage of these devices is for fluoroscopy studies for various anatomical regions of the human body.
Under some conditions during high doses procedures the cumulative air kerma display may reach its maximum capability and fail to display the accrued value.
An Important: Electronic Product Radiation Warning notification was sent to all consignees. The letters described the reason for the recall and identified the affected product. The system software will be modified to allow the shift of the decimal to one position to the right allowing for a display of 99999.9 mGy. This will allow for the retention of the resolution until such time as the system exceeds the 9999.99 mGy range. A Toshiba Service person will contact customers when the software is available. Installed systems with the current version of software ( version 4.23) will begin to receive the corrected software April 2011. Previous versions of the software will begin to receive corrected software June 2011. The software will be provided free of charge. Questions related to the letter should be directed to the Regulatory Affairs Department at 800-421-1968.
Nationwide Distribution
220 units Nationwide