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Recalls from FUJIFILM Healthcare Americas Corporation

Recalls from FUJIFILM Healthcare Americas Corporation filed with the FDA, USDA FSIS, CPSC or NHTSA, newest first. Company page 2 recalls Each recall is dated by the day its recall page names (how recalls are dated).
Agency
Risk level
Status
Date
Sold in

1 recall that day

FUJIFILM Synapse PACS Software

The software may cause the ruler measurement to be inaccurate.

Moderate risk, FDA, Software defect

1 recall that day

FUJIFILM FDR Visionary Suite

The FDR Visionary Suite X-ray high-voltage generator can overheat and damage parts, possibly causing smoke.

Moderate risk, FDA, Device defect