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All product recalls associated with FUJIFILM Healthcare Americas Corporation.
Total Recalls
22
Past Year
3
Class I (Serious)
0
Most Recent
Sep 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
It was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the shaft was broken while being operated toward the front while lifting.
Devices had an unapproved slabbing software function enabled for use.
The incorrect computed patient age is showing in VX for patients less than 3 months old.