EXTENSION SET
Report
- Report Number
- 1416980-2013-16072
- Event Type
- Injury
- Date Received
- June 20, 2013
- Date of Event
- May 23, 2013
- Report Date
- May 29, 2013
- Manufacturer
- BAXTER HEALTHCARE - MOUNTAIN HOME
- Product Code
- KDJ
- PMA / PMN Number
- K925403
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- NURSE
Narratives
(B)(4). A BATCH REVIEW WAS CONDUCTED FOR POTENTIALLY ASSOCIATED LOT NUMBERS H13B26089 AND H13B13061 AND NO EXCEPTIONS WERE OBSERVED THAT WERE RELATED TO THE REPORTED CONDITION. SHOULD RELEVANT ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED.
(B)(4). ON AN UNREPORTED DATE, THE PATIENT DIED. THE CAUSE OF DEATH WAS UNKNOWN. IT WAS NOT REPORTED IF AN AUTOPSY WAS PERFORMED. NO ADDITIONAL INFORMATION IS AVAILABLE.
(B)(4). UPON FURTHER INVESTIGATION IT WAS DETERMINED THAT THE EVENT OF PATIENT DEATH WAS REPORTED IN ERROR.
(B)(4). SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. SAME PATIENT AS (B)(4).
THIS IS REPORT 3 OF 4. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE PATIENT WAS HOSPITALIZED FOR SIX DAYS. THE PATIENT WAS TREATED CEFTAZIDIME (DOSE, ROUTE UNKNOWN). PD CATHETER PULLED AND THE PATIENT PLACED ON HEMODIALYSIS. PER THE RN AND PATIENT, NO DEFECTIVE PACKAGING OR DRY MINICAP WAS OBSERVED. THE CAUSE WAS UNKNOWN. PER THE RN, THESE EVENTS WERE UNRELATED TO BAXTER DEVICES OR SOLUTIONS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 281146 | EXTENSION SET | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE | KDJ | BAXTER HEALTHCARE - MOUNTAIN HOME |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 25 YR | Death| H| R | DIANEAL LOW CAL |