FLEXICAP
Report
- Report Number
- 1416980-2013-11235
- Event Type
- Injury
- Date Received
- May 3, 2013
- Date of Event
- March 19, 2013
- Report Date
- April 10, 2013
- Manufacturer
- BAXTER HEALTHCARE - SWINFORD
- Product Code
- KDJ
- PMA / PMN Number
- K972579
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- ID, US
- Reporter Occupation
- NURSE
Narratives
(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS FOR POTENTIALLY ASSOCIATED LOT NUMBER, 12I18H25 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 BECOMES AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. THIS IS THE SAME PATIENT AS (B)(4).
(B)(4): THE CAUSE OF PERITONITIS WAS UNKNOWN. ON AN UNREPORTED DATE, THE PATIENT WAS RETRAINED ON A PROPER ASEPTIC TECHNIQUE. THE PATIENT RECOVERED FROM PERITONITIS.
THE CULTURE WAS PERFORMED ON (B)(6) 2013.
THIS IS REPORT 3 OF 4. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE PATIENT HAD SYMPTOMS OF ABDOMINAL PAIN AND CLOUDY EFFLUENT. THE PATIENT WAS TREATED WITH ANCEF 1500 MILLIGRAMS INTRAPERITONEAL (IP) DAILY FOR 3 DAYS AND GENTAMYCIN 40 MILLIGRAM IP DAILY. AFTER CULTURES RESULTS WERE NEGATIVE, ANCEF WAS STARTED AS 1 GRAM DAILY IP FOR 5 DAYS. THE PATIENT IS CONSIDERED TO BE RECOVERED FROM THIS EVENT AND THE CAUSE OF PERITONITIS IS UNKNOWN. PD THERAPY WAS ONGOING DURING THE EVENT OF PERITONITIS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 193984 | FLEXICAP | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE | KDJ | BAXTER HEALTHCARE - SWINFORD |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 59 YR | Required Intervention | AMBUFLEX, EXTRANEAL |