FDA.reportPublic FDA data

MAUDE MDR 1813797

MDR report key
1813797
Report number
MW5017186
Event key
0
Event type
3
Date of event
2010-08-19
Date received
2010-08-19
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
109
Health professional
3
Initial report to FDA
3
Event location
0

Manufacturer Contact#

Report source
P
Manufacturer link flag
N

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1CERNER BRIDGE MEDPOINTMEDPOINT SYSTEM MANAGERCERNER BRIDGENZH Y

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12010-08-190

Event Narratives#

D

Patient 1

ERROR IDENTIFIED IN (B)(4) -BARCODING- DATABASE. ON LOADING A NEW PRODUCT IN OUR FORMULARY, THE DATABASE AUTOPOPULATED THE "DESCRIPTION" FIELD WITH "EPINEPHRINE" FOR THE PHARMEDIUM PRODUCTS FOR NOREPINEPHRINE, (B)(4) AND (B)(4). OUR CERNER BRIDGE VERSION IS (B)(4) WITH DATABASE VERSION (B)(4).