FLEXICAP
Report
- Report Number
- 1416980-2014-24991
- Event Type
- Injury
- Date Received
- August 1, 2014
- Report Date
- July 9, 2014
- Manufacturer
- BAXTER HEALTHCARE - SWINFORD
- Product Code
- KDJ
- PMA / PMN Number
- K972579
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- NURSE
Narratives
(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED FOR POTENTIALLY ASSOCIATED LOT NUMBERS 14A15H25 AND 13L12H25 WITH NO ISSUES NOTED DURING THE MANUFACTURING PROCESS. THERE WERE NO DEVIATIONS FROM STANDARD PROCEDURE AND NO EXCEPTIONS RELATED TO THE REPORTED CONDITION WERE NOTED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
(B)(4). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW-UP WILL BE SUBMITTED. SAME PATIENT AS (B)(4).
IT WAS REPORTED THAT A PERITONEAL DIALYSIS (PD) PATIENT EXPERIENCED PERITONITIS. ON AN UNREPORTED DATE, THE PATIENT WAS ADMITTED TO THE HOSPITAL FOR OTHER INDICATIONS. ON AN UNREPORTED DATE, DURING HOSPITALIZATION, THE PATIENT DEVELOPED PERITONITIS. THE CAUSE OF THE PERITONITIS EVENT WAS UNKNOWN. THE PATIENT WAS TREATED FOR THE PERITONITIS WITH FORTAZ, INTRAPERITONEALLY(IP) (DOSE AND FREQUENCY NOT REPORTED). IT WAS NOT REPORTED WHETHER THE PERITONITIS EVENT PROLONGED THE PATIENT¿S HOSPITALIZATION. AT THE TIME OF THIS REPORT, THE PATIENT WAS RECOVERING FROM THIS PERITONITIS EVENT. ADDITIONAL INFORMATION WAS REQUESTED BUT IS NOT AVAILABLE. THIS IS REPORT 3 OF 4 INVOLVED IN THIS PERITONITIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 450864 | FLEXICAP | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE | KDJ | BAXTER HEALTHCARE - SWINFORD |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention | DIANEAL SOLUTION, MINICAP TRANSFER SET, MINICAP| HOMECHOICE AUTOMATED PD SET WITH CASSETTE |