FDA Adverse Event Malfunction Summary report: N

MINICAP

MDR report key: 4171584 · Received October 14, 2014

Report

Report Number
1416980-2014-35894
Event Type
Malfunction
Date Received
October 14, 2014
Report Date
September 19, 2014
Manufacturer
BAXTER HEALTHCARE - GUANGZHOU
Product Code
KDI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). EVALUATION SUMMARY: AN EXTRA, UNREPORTED SAMPLE WAS RECEIVED ALONG WITH THE SAMPLE FOR (B)(4). A VISUAL INSPECTION FOUND THAT THIS EXTRA SAMPLE HAD BEEN OPENED FOR TWO MONTHS AND ITS IODINE SPONGE WAS DRY. THE IODINE CONTENT OF THE SAMPLE WAS EVALUATED AND FOUND TO MEET SPECIFICATION. THE DRY SPONGE CONDITION WAS VERIFIED FOR THE OPEN SAMPLE. A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED WITH NO ISSUES NOTED DURING THE MANUFACTURING PROCESS. THERE WERE NO DEVIATIONS FROM STANDARD PROCEDURE AND NO EXCEPTIONS RELATED TO THE REPORTED CONDITION WERE NOTED. THE CAUSE OF THE PROBLEM COULD NOT BE DETERMINED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

COMPLAINT NO: (B)(4). THE PATIENT'S ADDRESS IS "(B)(6)". THE DEVICE HAS BEEN RECEIVED AND THE EVALUATION IS IN PROGRESS. UPON COMPLETION OF THE INVESTIGATION, OR IF ANY ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

UPON EVALUATION OF A RETURNED SAMPLE, IT WAS NOTED THAT THE SPONGE OF THE MINICAP WAS DRY. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS IS REPORT 3 OF 17.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
649938 MINICAP DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - GUANGZHOU GM1309010

Patients

Seq Age Sex Outcome Treatment
1