FDA Adverse Event Injury Summary report: N

PUMP, INSULIN, 712 NA PURPLE

MDR report key: 562065 · Received December 28, 2004

Report

Report Number
2032227-2004-02378
Event Type
Injury
Date Received
December 28, 2004
Date of Event
December 7, 2004
Report Date
December 7, 2004
Manufacturer
MEDTRONIC MINIMED
Product Code
LZG
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

CUSTOMER REPORTED BEING HOSPITALIZED DUE TO DRUG INTERACTION AND HBG AS PER MD. CUSTOMER HAD HBG FOR 2 DAYS AND STARTED VALIUM SAME DAY. INSTRUCTED CUSTOMER TO MONITOR BG, EXPLAINED 2 HBG RULE AND CALL BACK FOR HP TEST WHEN CLAMP ARRIVES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PUMP, INSULIN, 712 NA PURPLE INFUSION PUMP LZG MEDTRONIC MINIMED MMT-712NAP *

Patients

Seq Age Sex Outcome Treatment
1 61 YR Hospitalization