FDA Adverse Event Malfunction Summary report: N

SPECTRUM INFUSION PUMP

MDR report key: 2820456 · Received October 4, 2012

Report

Report Number
1314492-2012-00343
Event Type
Malfunction
Date Received
October 4, 2012
Report Date
August 8, 2012
Manufacturer
SIGMA INTL.
Product Code
FRN
PMA / PMN Number
K042121
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). SIGMA EVALUATED THE DEVICE IN QUESTION AND A STUCK #8 KEY COULD NOT BE REPRODUCED. HOWEVER, THE EVAL FOUND THE 1ST SOFTKEY, ON/OFF, #0 AND (.) KEYS TO BE INOPERABLE CAUSED BY A FAILED KEYPAD. ALL OTHER KEYS PERFORMED AS EXPECTED AND NO KEYS RESULTED IN AN INCORRECT RESPONSE OR DOUBLE ENTRY.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE #8 KEY ON A PUMP KEYPAD IS STUCK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SPECTRUM INFUSION PUMP INFUSION PUMP FRN SIGMA INTL. 35700

Patients

Seq Age Sex Outcome Treatment
1