Overview of recall records associated with FUJIFILM Healthcare Americas Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 1.
It was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might continue to be supplied to…
This page summarizes recall records in which the official source identifies FUJIFILM Healthcare Americas 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.
