SURDIAL X
Report
- Report Number
- 3016250252-2021-00013
- Event Type
- Malfunction
- Date Received
- August 5, 2021
- Date of Event
- April 8, 2021
- Report Date
- December 20, 2022
- Manufacturer
- SHIBUYA (SBY)
- Product Code
- KDI
- PMA / PMN Number
- K182940
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
THE MANUFACTURER EVALUATED THE DEVICE IN QUESTION AND DETERMINED THAT THE DEVICE IS SIMILAR TO 510K# K182940, THEREFORE MDR REPORTABILITY WAS DETEMINED ON JULY 8, 2021.
IT WAS REPORTED THAT DURING A DIALYSIS TREATMENT ON (B)(6). THE NIPRO DIALYSIS MACHINE SURDIAL¿ X, BEARING SERIAL NUMBER (B)(6), REMOVED AN INCORRECT VOLUME OF FLUIDS FROM THE PATIENT. THE PATIENT CAME OFF THE DIALYSIS TREATMENT 0.6KG UNDER THE TARGET WEIGHT AND THE BLOOD PRESSURE DROPPED SIGNIFICANTLY TO 100/67. NO FURTHER INFORMATION WAS PROVIDED.
THE MANUFACTURER EVALUATED THE DEVICE IN QUESTION AND DETERMINED THAT THE DEVICE IS SIMILAR TO 510K# K182940, THEREFORE MDR REPORTABILITY WAS DETEMINED ON JULY 8, 2021.
IT WAS REPORTED THAT DURING A DIALYSIS TREATMENT ON APRIL 8TH THE NIPRO DIALYSIS MACHINE SURDIAL¿ X, BEARING SERIAL NUMBER (B)(4), REMOVED AN INCORRECT VOLUME OF FLUIDS FROM THE PATIENT. THE PATIENT CAME OFF THE DIALYSIS TREATMENT 0.6KG UNDER THE TARGET WEIGHT AND THE BLOOD PRESSURE DROPPED SIGNIFICANTLY TO 100/67. NO FURTHER INFORMATION WAS PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1176050 | SURDIAL X | HEMODIALYSIS MACHINE | KDI | SHIBUYA (SBY) | SURDIAL-X2-HD-UJ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown | Other |