Toshiba DRAD-3000E FPD Wireless System Product Usage The DRAD-3000 is intended for use with the ceiling-suspended tube support, high voltage generator, and bucky stand or bucky table incorporating a fixed or detachable (portable) flat panel detector for radiography of the head, chest, abdomen, spine, neck, and limbs. This system is used for image acquisition, image display and transmission/output or images to external devices.
FDA Recall Z-1175-2016 · Posted 2016-03-21
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Recalling FirmToshiba American Medical Systems Inc
Recall StatusTerminated
Product CodeJAA
Date Initiated2016-01-14
Date Terminated2017-02-24
Product Quantity28
Reason for Recall
When a user performed radiography using the wireless FPD, a message window appeared on the
monitor stating that imaging transmission was not completed with no radiographic image. It also indicated to select the "OK" button to re-acquire the image data or to select the'Cancel" button to cancel the re-acquisition. As instructed the user selected "OK" and the same message
window appeared. This same operation was repeated several times with the identical result - no image. Finally, the user selected "Cancel" and the re-acquisition was terminated.
Firm Action
Toshiba's planned action:
1."Toshiba America Medical Systems, Inc. (TAMS) will advise contact customers to stop using the system if any abnormalities are found using the system.
2. TAMS will install the software and perform testing to ensure the software update was effective.
3. The customer notification letter which includes a statement that TAMS
will without charge, remedy the defect or bring the product into
compliance.
CDRH approves the CAP subject to the following conditions:
1. Notification of all dealers and purchasers is to be made within 15
working days of receipt of this letter in the manner specified in 21 CFR
1003.21 and 1003.22. This office and the Food and Drug
Administration (FDA) district office coordinator noted below are to be
included in the notification.
2. TAMS will implement this CAP by June 30, 2016.
Customers with questions were advised to call 301-796-5910.
For questions regarding this recall call 714-730-5000.
Root Cause
Radiation Control for Health and Safety Act
Distribution Pattern
Nationwide distribution to PA, UT, FL, NY, LA, WV, NJ, OH, WI and TX.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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