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..
[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
Report Number | 1222895-2014-00008 |
MDR Report Key | 3902753 |
Report Source | 06 |
Date Received | 2014-05-09 |
Date of Report | 2014-04-25 |
Date of Event | 2014-04-22 |
Date Mfgr Received | 2014-04-28 |
Date Added to Maude | 2014-07-15 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | SANDRA LEE |
Manufacturer Street | 315 ENTERPRISE DR |
Manufacturer Phone | 6099366828 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BATTERY CHARGER, SINGLE BAY |
Generic Name | LIGHTING |
Product Code | EBZ |
Date Received | 2014-05-09 |
Catalog Number | 90523 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INTEGRA BURLINGTON, MA, INC. |
Manufacturer Address | BURLINGTON MA 01803 US 01803 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2014-05-09 |