BATTERY CHARGER, SINGLE BAY 90523

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2014-05-09 for BATTERY CHARGER, SINGLE BAY 90523 manufactured by Integra Burlington, Ma, Inc..

Event Text Entries

[4543983] Customer initially reports the battery charger device was not plugged in so rn plugged in to wall, then the unit experienced a large flash and a buzzing sound from the charging unit. Date: (b)(6) 2014 clinical supervisor reports that event occurred in the equipment room and no harm to personnel.
Patient Sequence No: 1, Text Type: D, B5


[11931180] To date the device involved in the reported incident has not been received for evaluation. An investigation has been initiated based on the reported info.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1222895-2014-00008
MDR Report Key3902753
Report Source06
Date Received2014-05-09
Date of Report2014-04-25
Date of Event2014-04-22
Date Mfgr Received2014-04-28
Date Added to Maude2014-07-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactSANDRA LEE
Manufacturer Street315 ENTERPRISE DR
Manufacturer Phone6099366828
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBATTERY CHARGER, SINGLE BAY
Generic NameLIGHTING
Product CodeEBZ
Date Received2014-05-09
Catalog Number90523
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA BURLINGTON, MA, INC.
Manufacturer AddressBURLINGTON MA 01803 US 01803


Patients

Patient NumberTreatmentOutcomeDate
10 2014-05-09

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