MINICAP TRANSFER SET
Report
- Report Number
- 1416980-2014-15032
- Event Type
- Injury
- Date Received
- May 9, 2014
- Date of Event
- April 12, 2014
- Report Date
- April 15, 2014
- Manufacturer
- BAXTER HEALTHCARE - MOUNTAIN HOME
- Product Code
- KDJ
- PMA / PMN Number
- K882498
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- NURSE
Narratives
(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED FOR POTENTIALLY ASSOCIATED LOT NUMBERS H13I04032, H13I10047, AND H13I27025 WITH NO ISSUES NOTED DURING THE MANUFACTURING PROCESS. THERE WERE NO DEVIATIONS FROM STANDARD PROCEDURE AND NO EXCEPTIONS RELATED TO THE REPORTED CONDITION. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW-UP WILL BE SUBMITTED. THIS IS THE SAME PATIENT AS (B)(4).
IT WAS REPORTED THAT A PERITONEAL DIALYSIS (PD) PATIENT (PT) EXPERIENCED PERITONITIS. THE CAUSE OF PERITONITIS WAS UNKNOWN. THREE DAYS PRIOR TO THE RECEIPT OF THIS REPORT, THE PT WAS HOSPITALIZED FOR THE EVENT. THE PT RECEIVED TREATMENT FOR THE PERITONITIS WITH CEFTAZIDIME (1 GRAM, INTRAPERITONEALLY (IP) FOR 10 DAYS) AND VANCOMYCIN (500MG, IP, EVERY OTHER DAY FOR 10 DAYS). SIX DAYS AFTER BEING ADMITTED TO THE HOSPITAL, THE PT WAS DISCHARGED. AT THE TIME OF THIS REPORT, THE PATIENT HAD RECOVERED FROM THE EVENT AND DIANEAL THERAPIES WERE ONGOING. THIS IS REPORT 2 OF 3 INVOLVED IN THIS PERITONITIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 281513 | MINICAP TRANSFER SET | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE | KDJ | BAXTER HEALTHCARE - MOUNTAIN HOME |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 27 YR | Hospitalization| R | HOMECHOICE AUTOMATED PD SET WITH CASSETTE| DIANEAL PD4, 2.5% AMBUFLEX| MINICAP| DIANEAL PD4, 4.25% AMBUFLEX| DIANEAL PD4, 1.5% AMBUFLEX |