Recall Z-2580-2021

Biodex Medical Systems, Inc. · initiated August 16, 2021

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Atomlab 500 Dose Calibrator Software 2.0.00 through Revision 2.0.08, inclusive Model: 086-330.

Codes / lots: Serial Number range:17081557-21062362 UDI: 00718175003305

Reason for recall

When deleting a previously entered custom isotope, the software deletes the isotope, but not the associated dial setting. Possible other stored custom isotopes may then have incorrect dial settings and may lead to an incorrect dose measurement and/or misadministration

FDA-determined cause: Software design

Action taken

Biodex issued Urgent Medical Deice Recall Letter on 8/16/21 via email. Letter states reason for recall, health risk and action to take: Review the dial settings associated with custom isotope and confirm they have not been changed. Compare the measured activity with a dose calibrator from another manufacturer The error can be immediately corrected by restarting the system. We recommend that you promptly download new software. The error is corrected in Software Revision 2.0.10. The corrected software upgrade is available as a download from the Biodex website at the following link Atomlab 500 Dose Calibrator Software Update v2.0.10 - Software Updates - Nuclear Medicine | Biodex. System registration is required for download. Please email us at supportservices@biodex.com to acknowledge receipt of this letter and confirm commitment to download the software update. To minimize risk of illness or injury, please download the software correction, as soon as possible. If you have any questions or require any additional information, please contact supportservices@biodex.com.

Details

Recall number
Z-2580-2021
Initiated
August 16, 2021
Terminated
May 30, 2024
Product code
KPT – Calibrator, Dose, Radionuclide
Quantity
829 units
Distribution
Nationwide Foreign: Austria Autralia Brazil CANADA Chile Colombia Croatia Cyprus Czech Republic Denmark Dominican Republic Ecuador Egypt France Hong Kong HUNGARY Iceland India Iraq Ireland ISRAEL Isreal Italy Japan JORDAN Kuwait Lebanon Libya Malaysia MALTA Mexico Morocco Netherlands New Zealand Oman Pakistan Palestine Panama Peru Philippines Poland Portugal PR Puerto Rico Qatar Romania Russia…
Recalling firm
Biodex Medical Systems, Inc., Shirley, NY

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2581-2021 Class IIAtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08, inclusive Model:…When deleting a previously entered custom isotope, the software deletes the isotope, but not the associated… 08/16/2021Terminated