FDA Adverse Event Summary report: N

CURLIN INFUSION PAINSMART IOD IV PUMP

MDR report key: 2143016 · Received June 21, 2011

Report

Report Number
1722139-2011-00102
Date Received
June 21, 2011
Report Date
June 21, 2011
Manufacturer
MOOG MEDICAL DEVICES GROUP
Product Code
FRN
PMA / PMN Number
K981816
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

METHOD: ACTUAL DEVICE FROM COMPLAINT WAS EVALUATED. CONCLUSION: DURING THE NON-FACTORY RECERTIFICATION (NFR) PROCESS AT AUTHORIZED 3RD PARTY FACILITIES, THE NFR SOFTWARE CHANGES THE CONFIGURATION OF THE PUMP TO 6000CMS SO THE OPERATOR CAN TEST THE DEVICE. IF THE NFR PROCESS IS INTERRUPTED IN ANY WAY (POWER LOSS, PUMP IS DISCONNECTED FROM THE PC RUNNING THE NFR, ETC.), THE RECERTIFICATION PROCESS IS STOPPED AND THE DEVICE CONFIGURATION REMAINS AS THE 6000CMS MODEL TYPE. THERE ARE INSTRUCTIONS IN THE SERVICE MANUAL TO CONTINUE WITH THE NFR PROCESS IF IT IS STOPPED FOR ANY REASON. THE CONFIGURATION IS RECOVERABLE AT ANY TIME UNLESS A DIFFERENT PUMP IS CONNECTED TO THE NFR, AT WHICH POINT THE PUMP THAT WAS DISCONNECTED REMAINS AT 6000 CMS CONFIGURATION. THE OPERATOR IN THIS CASE DID NOT FOLLOW THESE INSTRUCTIONS (PG. 23 OF TECHNICAL SERVICE MANUAL 350-9023). THE DEVICE EXTERIOR IS PAINSMART IOD, BUT THE DEVICE INTERNAL SOFTWARE SHOWS 6000CMS WHEN TURNED ON. THE DEVICE WAS NOT BEING USED BY A PATIENT, IT WAS RECEIVING THE ANNUAL RECERTIFICATION AT THE TIME.

Description of Event or Problem · 1

COMPLAINT DESCRIPTION: "LOST CONFIGURATION DURING NFR". PROBLEM FOUND DURING THE RECERTIFICATION (NFR) PROCESS. DEVICE WAS NOT ON A PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CURLIN INFUSION PAINSMART IOD IV PUMP FRN MOOG MEDICAL DEVICES GROUP

Patients

Seq Age Sex Outcome Treatment
1