SYNAPSE PACS
Report
- Report Number
- 3004972322-2020-00009
- Event Type
- Malfunction
- Date Received
- December 22, 2020
- Date of Event
- November 9, 2020
- Report Date
- April 12, 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
- MA, US
- Reporter Occupation
- PHYSICIAN
Narratives
FUJIFILM INITIATED A RECALL ON 03/02/2021 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 THE FDA, WHICH WAS CLASSIFIED AS CLASS II AND ASSIGNED RECALL NUMBER Z-1348-2021 ON 04/02/2021. NO FURTHER INVESTIGATION IS NECESSARY.
PATIENT INFORMATION: UNKNOWN. 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. IF ANY ADDITIONAL RELEVANT INFORMATION BECOMES AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. REF: INTERNAL COMPLAINT NUMBER (B)(4).
ON NOVEMBER 09, 2020 FUJIFILM MEDICAL SYSTEMS USA, INC. (FMSU) SERVICE DEPARTMENT RECEIVED A CUSTOMER INQUIRY FOR ASSISTANCE WITH SYNAPSE PACS POWERJACKET. THE POWERJACKET WINDOW CAN BECOME OUT OF SYNC AND DISPLAY THE DETAILS FOR THE PREVIOUSLY LOADED PATIENT. ON NOVEMBER 25, 2020 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.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1519983 | SYNAPSE PACS | SYNAPSE PACS | LLZ | N/A | N/A | 00854904006008 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |