Recall Z-3030-2026

FUJIFILM Healthcare Americas Corporation · initiated July 22, 2026

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

FUJIFILM Synapse PACS software v7.4.310; radiological image processing system

Codes / lots: UDI (01)00854904006008(10)0704310, Serial Numbers: CV-00272120, CV-0080080176, CV-01318490, CV-01-80102732, CV-80057523, CV-00494020-38

Reason for recall

Software issue may cause the ruler measurement to be inaccurate.

FDA-determined cause: Software design

Action taken

FUJIFILM issued an URGENT MEDICAL DEVICE CORRECTION to its consignees on 7/21/2026 via email. The notice explained the issue and how to identify it, risk to health, and requested the following: "ACTIONS TO BE TAKEN BY THE CUSTOMER/END-USER 1. Please post this notification on or near the Synapse PACs workstation. 2. Please complete and return the Field Action Verification Form attached to this communication. Responding with the information requested is essential for ensuring appropriate action is taken. 3. Please contact Technical Assistance Center (TAC) at 1-888-FUJIMED (1-888-385-4633) to open a service ticket. 4. Please report any known adverse events to FDA via MedWatch. Regarding this issue, Synapse PACS can safely be used by the end-user as long as: 5. The end-user is aware of the issue and, 6. Appropriate actions are taken when rendering a diagnosis for patients. The following workarounds can be used: 7. Perform M-mode ruler measurements on the ultrasound system and then transfer the study to Synapse PACS." For questions regarding this notice, please email hcusquality@fujifilm.com.

Details

Recall number
Z-3030-2026
Initiated
July 22, 2026
Posted by FDA
August 26, 2026
Product code
LLZ – System, Image Processing, Radiological
Quantity
6 units
Distribution
Worldwide - US Nationwide distribution in the states of NY, VA, KS, OR, OH, and the country of Australia.
Recalling firm
FUJIFILM Healthcare Americas Corporation, Lexington, MA

Official FDA recall record