FDA Adverse Event Malfunction Summary report: N

IPUMP PAIN MANAGEMENT SYSTEMUS VERSION

MDR report key: 1832473 · Received September 13, 2010

Report

Report Number
6000001-2010-03118
Event Type
Malfunction
Date Received
September 13, 2010
Date of Event
July 1, 2010
Report Date
August 18, 2010
Manufacturer
BAXTER HEALTHCARE - SINGAPORE
Product Code
FRN
PMA / PMN Number
K052973
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN RECEIVED BY BAXTER FOR EVALUATION. A FOLLOW UP MEDWATCH WILL BE SUBMITTED UPON COMPLETION OF BAXTER'S INVESTIGATION. (B)(4).

Additional Manufacturer Narrative · 1

THE REPORTED CONDITION OF OVERINFUSION WAS NOT CONFIRMED OR DUPLICATED. THE DEVICE SUCCESSFULLY PASSED THE PRE-ACCURACY TESTING. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE A FOLLOW UP MEDWATCH WILL BE SUBMITTED. COMPLAINT NO: (B)(4).

Additional Manufacturer Narrative · 1

BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED. THE DEVICE HAS NOT BEEN PREVIOUSLY SENT INTO SERVICE FOR THE REPORTED CONDITION OF "OVER-INFUSING." (B)(4).

Description of Event or Problem · 1

THE FACILITY REPRESENTATIVE REPORTED TO BAXTER (B)(4) TECHNICAL SERVICES ONE IPUMP THAT IS OVERINFUSING. THE REPORTED CONDITION OCCURRED DURING BIO-MED TESTING. ACCORDING TO THE HOSPITAL REPRESENTATIVE, NO PATIENT INJURY OR MEDICAL INTERVENTION HAD BEEN REPORTED RELATED TO THIS DEVICE. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IPUMP PAIN MANAGEMENT SYSTEMUS VERSION PUMP, INFUSION FRN BAXTER HEALTHCARE - SINGAPORE

Patients

Seq Age Sex Outcome Treatment
1