FDA Recall Terminated

Fujifilm Synapse PACS, Software versions: 4.0.xxx, 4.1.xxx, version 4.2.xxx, version 4.3.xxx Medical imaging and information management system, SYNAPSE allows the archiving and distribution of image information from all modalities

Recall: Z-0073-2017 · Initiated September 15, 2016

Recall

Recall Number
Z-0073-2017
Event Number
75192
Firm
Fujifilm Medical Systems U.S.A., Inc.
FEI Number
1000513161
Product Code
LLZ
Status
Terminated
Root Cause
Software design
Initiated
September 15, 2016
Terminated
February 20, 2019
Address
419 West Ave, Stamford, CT, 06902-6343

Description

Fujifilm Synapse PACS, Software versions: 4.0.xxx, 4.1.xxx, version 4.2.xxx, version 4.3.xxx Medical imaging and information management system, SYNAPSE allows the archiving and distribution of image information from all modalities

Reason

Image data for a patients image may not be correct

Action

The firm, FMSU, sent a "Medical Device Correction" letter dated September 15, 2016 to its customers. The letter describes the product, problem and actions to be taken. The firm will install a patch that corrects the issue (Synapse IPSS v1.3.1.0 Patch).Customers with Version 4.0 may upgrade to version 4.4 (will not require the patch) or upgrade to 4.1, 4.2, or 4.3 and install the patch. FMSU will install the patch on the server remotely if your site uses Active Monitoring. Your notification that the patch was installed will be your service ticket. For sites not using Active Monitoring, FMSU will schedule a time to install the patch on your server. Questions or concerns, contact the FUJIFILM Customer Support Center at 1-888-FUJIMED (1-800-385-4633) Option #1. International callers can access the FUJIFILM Customer Support Center by calling 1-203-602-3580.

Distribution

US Nationwide Distribution.

Quantity

251 units