Biodex Medical Systems, Inc. recalls AtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08, inclusive Model: 086-332

Recall date

August 16, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2581-2021

FDA classification

Class II

Brand / firm

Biodex Medical Systems, Inc.

Sold / distributed

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 Om…

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

AtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08, inclusive Model: 086-332