Z-1407-2025Class II

Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200

Name: Z-1407-2025 Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200
Creator: FUJIFILM Healthcare Americas Corporation
Published: 2025-02-11
License: https://open.fda.gov/license/

FUJIFILM Healthcare Americas Corporation / initiated 2025-02-11 / Open, Classified / root cause: software

FDA source

FUJIFILM Healthcare Americas Corporation began a recall of Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200 on 2025-02-11. FDA classified it as Class II and gives the reason as "The incorrect computed patient age is showing in VX for patients less than 3 months old". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as software.

Recall record

Recall number: Z-1407-2025
Classification: Class II
Status: Open, Classified
Initiated: 2025-02-11
Posted: 2025-03-20
Recalling firm: FUJIFILM Healthcare Americas Corporation
Product: Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.
Product code: LLZ System, Image Processing, Radiological
Reason for recall: The incorrect computed patient age is showing in VX for patients less than 3 months old.
Root cause tag: software
FDA root cause: Software change control
Action: On February 11, 2025 URGENT: MEDICAL DEVICE RECALL letters were sent to customers. ACTIONS TO BE TAKEN BY THE COMPANY Fujifilm will issue corrections for all impacted 7.4.x versions. The following patch releases will be made available: - 7.4.020 for 7.4.0x versions (immediately available) - 7.4.120 for 7.4.1x versions (available February 28, 2025) - 7.4.210 for 7.4.2x versions (available February 28,2025) ACTIONS THAT CAN BE TAKEN BY THE END-USER IMMEDIATELY Regarding this issue, Synapse PACS VX can safely be used by the end-user as long as; 1] the end-user is aware of the issue and, 2] takes appropriate actions when rendering a diagnosis for patients under 18 years of age. The following workarounds can be used: 1) The image acquisition date and date of birth are displayed on the Image. The end-user can use the dates to verify the age or, 2) Open the Series Viewer by double clicking on the thumbnail displayed on top the Synapse VX Image viewing window or the worklist. The Series Viewer Window will render the image on the server using the Server-side rendering (Zero Viewer component) which will calculate the age correctly. Alternatively, the user can switch to the Synapse PACS Zero Viewer/Thin Viewer (Server-side Rendering). The Synapse PACS Zero Viewer/Thin Viewer calculates the age correctly. ACTIONS TO BE TAKEN BY THE CUSTOMER/END-USER 1) 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. 2) Please contact Customer Service at 1-888-FUJIMED (1-888-385-4633) to schedule a patch update. Fujifilm regrets any inconvenience this action may cause and appreciates your understanding and cooperation. Please contact our field action coordinator, Jay Wigley, via email at [email protected], if you have any further questions regarding this field action. Please contact Technical Assistance Center (TAC) at 1-888-385-4622 or 1-888-FU
Quantity in commerce: 104 units (69 US, 35 OUS)
Distribution: Domestic: AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, LA, MA, MN, MO, MS, NC, NJ, NY, OH, OK, OR, TN, TX, VT, WA, WI, WV, WY. International: Australia, Belgium, Brazil, France, Germany, Portugal, UK
Product codes and lots: Model numbers: Synapse PACS 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200 Software Version Numbers: Synapse PACS 7.4.000, UDI: (01)00854904006008(10)0704000; Synapse PACS 7.4.001, UDI: (01)00854904006008(10)0704001; Synapse PACS 7.4.010, UDI: (01)00854904006008(10)0704010; Synapse PACS 7.4.100, UDI: (01)00854904006008(10)0704100; Synapse PACS 7.4.110, UDI: (01)00854904006008(10)0704110; Synapse PACS 7.4.200, UDI: (01)00854904006008(10)0704200.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1407-2025
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1407-2025	Class II	Ongoing	Voluntary: Firm initiated	2025-03-26	2025-03-20

Product code LLZ

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)