FDA Adverse Event Injury Summary report: N

MINICAP

MDR report key: 2073491 · Received May 1, 2011

Report

Report Number
1423500-2011-05256
Event Type
Injury
Date Received
May 1, 2011
Date of Event
March 1, 2011
Report Date
April 6, 2011
Manufacturer
BAXTER HEALTHCARE - CLEVELAND
Product Code
KDI
PMA / PMN Number
K895631
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MT, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS IS REPORT 2 OF 2 FOR THIS INCIDENCE OF PERITONITIS. AS THE PATIENT DISCARDS SUPPLIES AFTER EACH USE A SAMPLE WAS NOT AVAILABLE FOR EVALUATION. A FOLLOW UP WILL BE SUBMITTED AS INFORMATION BECOMES AVAILABLE.

Additional Manufacturer Narrative · 1

(B)(4). THE ROOT CAUSE OF THE REPORTED CONDITION OF PERITONITIS WAS UNDETERMINED. A BATCH REVIEW OF THE POTENTIALLY ASSOCIATED LOT NUMBER (GD879924) REVEALED NO EXCEPTIONS DURING THE MANUFACTURING PROCESS. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS.

Description of Event or Problem · 1

ON (B)(6) 2011 A CUSTOMER CONTACTED BAXTER AND VERBALIZED HE HAD JUST BEEN RELEASED FROM THE HOSPITAL. ON (B)(6) 2011 BAXTER'S GLOBAL PHARMACOVIGILENCE CONTACTED THE PATIENTS PERITONEAL DIALYSIS RN THAT ON AN UNKNOWN DATE THE PATIENT WAS DIAGNOSED WITH PERITONITIS. ON UNKNOWN DATE PD EFFLUENT CULTURES WERE TAKEN. THE PATIENT WAS HOSPITALIZED FROM (B)(6) 2011. SHE STATED THAT THE CAUSE OF THE PERITONITIS WAS MOST LIKELY FROM TOUCH CONTAMINATION. THERE WAS NO ALLEGATION AGAINST ANY BAXTER SOLUTION OR DEVICE. NO FURTHER INFORMATION AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MINICAP DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - CLEVELAND

Patients

Seq Age Sex Outcome Treatment
1 60 YR Hospitalization| R DIANEAL LOCAL (PD4) AMBUFLEX| HOME CHOICE CYCLER