Best Theratronics cabinet x-ray systems intended for use in the irradiation of blood and recall — FDA Z-2251-2016
It was discovered that both the new device and the predicate device failed to comply with performance standard.
Overview of recall records associated with BEST THERATRONICS LTD., including dates, categories and classifications where available.
Classification mix: Class II: 1.
It was discovered that both the new device and the predicate device failed to comply with performance standard.
This page summarizes recall records in which the official source identifies BEST THERATRONICS LTD. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.