FDA Adverse Event Malfunction Summary report: N

INTERMATE

MDR report key: 2103047 · Received May 25, 2011

Report

Report Number
6000001-2011-04630
Event Type
Malfunction
Date Received
May 25, 2011
Date of Event
May 1, 2011
Report Date
May 6, 2011
Manufacturer
BAXTER HEALTHCARE - IRVINE
Product Code
FRN
PMA / PMN Number
K910425
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). DEVICE EVALUATION: ONE SAMPLE WAS RECEIVED BY BAXTER FOR EVALUATION. VISUAL EXAMINATION AND FUNCTIONAL TESTING OF THE UNIT DID NOT CONFIRM THE LEAK. THIS IS A SINGLE USE DEVICE AND WILL NOT BE REPAIRED. NO OTHER OBSERVATION WAS FOUND ON THE UNIT. A BATCH REVIEW WAS CONDUCTED AND NO ISSUES WERE FOUND RELATED TO THE REPORTED CONDITION DURING THE MANUFACTURE OF THE LOT. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. THE ROOT CAUSE WAS NOT IDENTIFIED. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED.

Additional Manufacturer Narrative · 1

(B)(4). ADDITIONAL NARRATIVE: PER THE CUSTOMER, THIS DEVICE IS NOT AVAILABLE FOR EVALUATION. THEREFORE, THE RESULTS OF EVALUATION COULD NOT BE COMPLETED AND THE REPORTED CONDITION COULD NOT BE CONFIRMED. SHOULD THE DEVICE AND/OR ANY ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED

Description of Event or Problem · 1

BAXTER CANADA RECEIVED A REPORT INVOLVING THE CE INTERMATE DEVICE. THE QUALITY SPECIALIST REPORTED THAT THERE WAS A LEAK FROM BLUE WINGED LUER CAP, FOUND AFTER COMPOUNDING, CONTAINS PAMIDRONATE. THE PROCESS STEP WAS BEFORE USE, THEREFORE THERE WAS NO PATIENT INVOLVEMENT. THIS WILL REFERENCE REPORT 2 OF 2 FOR THE FACILITY, AS THE FACILITY REPORTED 2 DEVICES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INTERMATE PUMP, INFUSION FRN BAXTER HEALTHCARE - IRVINE 11A039

Patients

Seq Age Sex Outcome Treatment
1 PAMIDRONATE