HOMECHOICE AUTOMATED PD SET WITH CASSETTE
Report
- Report Number
- 1416980-2013-19954
- Event Type
- Injury
- Date Received
- July 29, 2013
- Date of Event
- January 22, 2013
- Report Date
- July 2, 2013
- Manufacturer
- BAXTER HEALTHCARE - MOUNTAIN HOME
- Product Code
- FKX
- PMA / PMN Number
- K923065
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- NURSE
Narratives
(B)(4). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. (B)(4).
(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS FOR POTENTIALLY ASSOCIATED LOT NUMBERS H12I15021 AND H12J20012 WAS PERFORMED 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.
IT WAS REPORTED THAT A PERITONEAL DIALYSIS (PD) PATIENT EXPERIENCED PERITONITIS WHILE IN THE HOSPITAL FOR SEVERE BACK PAIN. THE NURSE REPORTED THE CAUSE OF THE PERITONITIS WAS DIARRHEA WHICH HAD CROSSED OVER THE PERITONEAL MEMBRANE. TREATMENT FOR THE PERITONITIS INCLUDED ZYBOX, ORAL (DOSE AND FREQUENCY NOT REPORTED). ON AN UNREPORTED DATE, THE PATIENT WAS DISCHARGED FROM THE HOSPITAL. AT THE TIME OF THE INITIAL REPORT, THE PATIENT WAS NOT RECOVERED FROM THE PERITONITIS EVENT. THIS IS REPORT 1 OF 3 INVOLVED IN THIS PERITONITIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 352940 | HOMECHOICE AUTOMATED PD SET WITH CASSETTE | SYSTEM, PERITONEAL, AUTOMATIC DELIVERY | FKX | BAXTER HEALTHCARE - MOUNTAIN HOME |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 49 YR | Required Intervention | DIANEAL PD4, 2.5% AMBUFLEX, LOW CALCIUM| MINICAP TRANSFER SET| MINICAP| DIANEAL PD4, 4.25% AMBUFLEX, LOW CALCIUM |