RENAL - DISPOSABLE
Report
- Report Number
- 1423500-2010-06385
- Event Type
- Injury
- Date Received
- November 30, 2010
- Date of Event
- November 1, 2010
- Report Date
- November 8, 2010
- Product Code
- KDJ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN
- Reporter Occupation
- NURSE
Narratives
(B)(4). THE DEVICES INVOLVED IN THE INCIDENT WERE UNKNOWN. AS THE DATE OF ONSET OF THIS PERITONITIS EPISODE IS UNKNOWN AND PATIENTS DISCARD SUPPLIES AFTER EACH THERAPY, THE SAMPLE WAS NOT REQUESTED. A 510(K) NUMBER WILL NOT BE PROVIDED IN THE MDR AS THE PRODUCT CODE AND LOT NUMBER ARE UNKNOWN. SINCE THE LOT NUMBER IS UNKNOWN, A BATCH REVIEW WILL NOT BE PERFORMED. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTION IS REQUIRED.
THIS IS A SPONTANEOUS REPORT BY A NURSE FROM (B)(6) OF CONSTIPATION AND PERITONITIS IN A PATIENT COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. ON AN UNREPORTED DATE, THE PATIENT DEVELOPED CONSTIPATION. ON (B)(6) 2010, THE PATIENT WAS DIAGNOSED WITH PERITONITIS. THE CAUSE OF THE PERITONITIS WAS CONSTIPATION. ON (B)(6) 2010, THE PATIENT BEGAN REMEDIAL THERAPY WITH SUPACEF (750MG, TWICE A DAY, IP), GENTAMYCIN (80MG, LOADING DOSE, IP), GENTAMYCIN (40MG, DAILY, IP) AND HEPARIN (2ML, LOADING DOSE, IP). DIANEAL THERAPY WAS ONGOING, AS WAS REMEDIAL TREATMENT WITH SUPACEF AND GENTAMYCIN. THE PERITONITIS WAS RESOLVING. THE OUTCOME FOR THE CONSTIPATION WAS UNKNOWN. THE REPORTER BELIEVED THAT THE PERITONITIS WAS NOT RELATED TO DIANEAL THERAPY. AN OPINION OF CAUSALITY WAS NOT REPORTED FOR THE EVENT OF CONSTIPATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | RENAL - DISPOSABLE | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE | KDJ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 73 YR | Required Intervention | DIANEAL PD2 ULTRABAG |