FDA Adverse Event Injury Summary report: N

EXTENSION SET

MDR report key: 3181111 · Received June 20, 2013

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

Additional Manufacturer Narrative · 1

(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.

Additional Manufacturer Narrative · 1

(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.

Additional Manufacturer Narrative · 1

(B)(4). UPON FURTHER INVESTIGATION IT WAS DETERMINED THAT THE EVENT OF PATIENT DEATH WAS REPORTED IN ERROR.

Additional Manufacturer Narrative · 1

(B)(4). SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. SAME PATIENT AS (B)(4).

Description of Event or Problem · 1

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