FDA Adverse Event Injury Summary report: N

NI

MDR report key: 17497520 · Received August 10, 2023

Report

Report Number
1416980-2023-04006
Event Type
Injury
Date Received
August 10, 2023
Report Date
August 10, 2023
Manufacturer
BAXTER HEALTHCARE CORPORATION
Product Code
KDJ
PMA / PMN Number
NI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

E1: INITIAL REPORTER ADDRESS: (B)(6). STUDY ARTICLE: EL SHAMY, O., ATTALAH, S., SHARMA, S., AND URIBARRI, J. "COMPARING THE EFFECT OF PERITONEAL DIALYSIS CYCLER TYPE ON PATIENT-REPORTED SATISFACTION, SUPPORT NEEDS AND TREATMENTS". BMC NEPHROLOGY, (2002) 23:217 1 ¿ 5. HTTPS://DOI.ORG/10.1186/S12882-022-02854-Z. THE DEVICE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN; THEREFORE, A DEVICE ANALYSIS COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 0

A STUDY WAS PERFORMED IN WHICH SEVEN AUTOMATED PERITONEAL DIALYSIS (PD) PATIENTS EXPERIENCED PERITONITIS. THREE OF THE PATIENTS PRESENTED TO THE EMERGENCY ROOM AND WERE HOSPITALIZED FOR THE EVENTS. THE CAUSE, TREATMENT, PATIENT OUTCOMES AND ACTION TAKEN WITH PD THERAPY WERE NOT REPORTED. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1279393 NI SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE CORPORATION NA NI

Patients

Seq Age Sex Outcome Treatment
1 Unknown Hospitalization HOMECHOICE PRO CYCLER