Overview of recall records associated with Roche Diagnostics Corporation, including dates, categories and classifications where available.
Classification mix: Class III: 2, Class II: 2.
Calibration failures with Std.E, Sens.E, or Dup.E error due to atypical reaction kinetics and quality control failures have occurred due to contamination of R1 reagent with R3 reagent.
There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument.
There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument.
Using the following versions of cobas infinity software (2.0 thorough 2.5), there is a potential where the results from the first sample subsequent to the bottle change, (when using the…
This page summarizes recall records in which the official source identifies Roche Diagnostics Corporation 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.
