FDA Adverse Event Malfunction Summary report: N

MINICAP

MDR report key: 2142085 · Received June 28, 2011

Report

Report Number
1423500-2011-08420
Event Type
Malfunction
Date Received
June 28, 2011
Date of Event
May 31, 2011
Report Date
June 3, 2011
Manufacturer
BAXTER HEALTHCARE - SAO PAULO
Product Code
KDI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CI
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4)

Additional Manufacturer Narrative · 1

(B)(4).ALTHOUGH THE SAMPLE WAS NOT AVAILABLE, THE ROOT CAUSE WAS RELATED TO A PUNCTUAL FAILURE ON THE SENSOR THAT MONITORS THE INDIVIDUAL PACKING PROCESS AND OPERATIONAL FAILURE ON THIS PROCESS. A BATCH REVIEW WAS CONDUCTED AND NO ISSUES WERE FOUND RELATED TO THE REPORTED CONDITION DURING THE MANUFACTURE OF THE LOT. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED.

Additional Manufacturer Narrative · 1

(B)(4). A PICTURE IS AVAILABLE IS FOR EVALUATION. A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF BAXTER'S INVESTIGATION, OR IF ANY ADDITIONAL INFORMATION IS RECEIVED. A 510(K) NUMBER WILL NOT BE PROVIDED IN THE EMDR AS THIS PRODUCT IS MANUFACTURED FOR DISTRIBUTION OUTSIDE OF THE U.S. AND DOES NOT HAVE A 510(K) NUMBER. HOWEVER, IT IS BEING REPORTED BECAUSE IT IS THE SAME OR SIMILAR TO THE PRODUCT DISTRIBUTED WITHIN THE U.S.

Description of Event or Problem · 1

THIS IS AN INTERNATIONAL REPORT OF A MINI CAP THAT WAS MISSING FROM THE PACKAGING. THE PRODUCT HAS NOT BEEN USED ON PATIENTS. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION INDICATED AT THE TIME OF THE INITIAL REPORT.

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 - SAO PAULO PS38F5

Patients

Seq Age Sex Outcome Treatment
1