FDA Adverse Event Malfunction Summary report: N

SYNAPSE PACS

MDR report key: 11624344 · Received April 6, 2021

Report

Report Number
3004972322-2021-00007
Event Type
Malfunction
Date Received
April 6, 2021
Date of Event
March 12, 2021
Report Date
April 6, 2021
Product Code
LLZ
UDI-DI
00854904006008
PMA / PMN Number
K160108
Removal / Correction Number
SEE H10
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 1

THE ISSUE WAS EVALUATED AND REPLICATED IN THE FMSU LAB; THE CAUSE WAS TRACED TO A SOFTWARE CONFIGURATION. THIS ISSUE IS VERY RARE AND REQUIRES MANY TRIES WITH LARGE STUDIES TO REPRODUCE; IT IS CONSIDERED TO BE A VERY RARE OCCURRENCE IN A CLINICAL ENVIRONMENT. FUJIFILM INITIATED A RECALL ON 3/2/2021 TO ALERT CUSTOMERS OF SEVERAL PATIENT MISMATCH ISSUES EXISTING IN ALL SYNAPSE PACS 5 VERSIONS UP TO 5.7.210. FUJIFILM SUBMITTED C&R REPORT (1000513161-03/11/2021-001-C) TO FDA, WHICH HAS BEEN CLASSIFIED AS CLASS II AND ASSIGNED RECALL NUMBER Z-1348-2021. IF ANY ADDITIONAL RELEVANT INFORMATION BECOMES AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. REF: INTERNAL COMPLAINT NUMBER (B)(4).

Description of Event or Problem · 1

ON MARCH 15, 2021 FUJIFILM MEDICAL SYSTEMS USA, INC. (FMSU) WAS MADE AWARE OF AN INCIDENT WITH SYNAPSE PACS. WHEN A USER OPENS A STUDY WITH AN URL-CALL FROM THEIR HIS (SAP), IMAGES ARE SHOWN FROM PATIENT A BUT THE INFORMATION PANE SHOWS STUDIES FROM PATIENT B. ON (B)(6) 2021 A RISK ASSESSMENT WAS PERFORMED TO INVESTIGATE THE RISK TO PATIENT SAFETY. THERE WAS NO PATIENT IMPACT, SERIOUS INJURY OR DEATH ASSOCIATED WITH THIS EVENT. THE ISSUE IS CONSIDERED HIGHLY DETECTABLE BY A HEALTHCARE PROFESSIONAL; HOWEVER THIS REPORT IS BEING SUBMITTED IN ABUNDANCE OF CAUTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
522083 SYNAPSE PACS SYNAPSE PACS LLZ N/A N/A 00854904006008

Patients

Seq Age Sex Outcome Treatment
1