FDAAugust 16, 2021device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

biodex medical systemsbiodexbiodex medical

UPCs

00718175003329

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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