Xstrahl Treatment applicator for Gulmay Medical 150 or Xstrahl 150 superficial X-ray therapy recall — FDA Z-0389-2022
Base plate may detach from the main body of the treatment applicator.
Overview of recall records associated with Xstrahl Limited, including dates, categories and classifications where available.
Classification mix: Class II: 2.
Base plate may detach from the main body of the treatment applicator.
If a saved treatment plan with 2 opposing beams is edited prior to approval, then Beam 2 is not updated with the changed parameters upon selecting save, resulting in error messages during…
This page summarizes recall records in which the official source identifies Xstrahl Limited 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.