DYND70800

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-01-26 for DYND70800 manufactured by Medline Industries.

Event Text Entries

[66147221] It was reported staff found a clipper base charred after a weekend off. There was no injury as a result of the incident. It was determined that the device was part of a corrective action that took place in 2015. It is unknown why the facility was using the recalled device. We have followed up with them to assure they do not continue to use any recalled devices. Due to the reported incident and in an abundance of caution, this medwatch is being filed.
Patient Sequence No: 1, Text Type: N, H10


[66147222] It was reported a clipper charger base caught fire.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1417592-2017-00002
MDR Report Key6280777
Date Received2017-01-26
Date of Report2017-01-26
Device Manufacturer Date2013-06-01
Date Added to Maude2017-01-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. MEGAN DEBUS
Manufacturer StreetTHREE LAKES DRIVE
Manufacturer CityNORTHFIELD IL 60093
Manufacturer CountryUS
Manufacturer Postal60093
Manufacturer Phone8477703962
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Generic NameSURGICAL CLIPPER CHARGER BASE
Product CodeLWK
Date Received2017-01-26
Catalog NumberDYND70800
Lot Number13F1
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDLINE INDUSTRIES
Manufacturer AddressTHREE LAKES DRIVE NORTHFIELD IL 60093 US 60093


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-01-26

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