Arkray Factory USA AUTION HYBRID AU-4050 recall — FDA Z-1850-2019
This correction is being initiated due to a software issue which results in the possibility of incorrect patient information being assigned to sample results when the following rare…
Overview of recall records associated with Arkray Factory USA, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
This correction is being initiated due to a software issue which results in the possibility of incorrect patient information being assigned to sample results when the following rare…
This page summarizes recall records in which the official source identifies Arkray Factory USA, Inc. 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.