LED HEADLIGHT W/BATTERIES & AC/DC POWER SUPPLY - US 90520US

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-16 for LED HEADLIGHT W/BATTERIES & AC/DC POWER SUPPLY - US 90520US manufactured by Integra York, Pa Inc..

Event Text Entries

[117570406] The device was not yet returned to the manufacturer for analysis. The plant investigation is in progress and a supplemental medwatch report will be submitted upon completion of the investigation.
Patient Sequence No: 1, Text Type: N, H10


[117570407] A customer reported that on (b)(6) 2018, a 90520us led headlight when the fan kicks on the light goes dim and the fan makes a lot of noise. The headlight gets overheated. It is unknown if there was any patient contact, injury and delay in surgery. Additional information has been requested. No other clinical information received.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2523190-2018-00103
MDR Report Key7790718
Date Received2018-08-16
Date of Report2018-08-08
Date of Event2018-08-08
Date Mfgr Received2018-10-18
Device Manufacturer Date2016-03-21
Date Added to Maude2018-08-16
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 FDA3
Event Location3
Manufacturer ContactUSER KIMBERLY SHELLY
Manufacturer Street311 ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal08536
Manufacturer Phone6099362393
Manufacturer G1INTEGRA YORK, PA INC.
Manufacturer Street589 DAVIES DRIVE
Manufacturer CityYORK PA 17402
Manufacturer CountryUS
Manufacturer Postal Code17402
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameLED HEADLIGHT W/BATTERIES & AC/DC POWER SUPPLY - US
Generic NameLIGHTING
Product CodeFSR
Date Received2018-08-16
Returned To Mfg2018-09-21
Catalog Number90520US
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA YORK, PA INC.
Manufacturer Address589 DAVIES DRIVE 589 DAVIES DRIVE YORK PA 17402 US 17402


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.