BLUE 80 569051999

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-12-05 for BLUE 80 569051999 manufactured by Maquet Sas.

Event Text Entries

[178203079] The issue is being investigated by manufacturing site. Device not returned to manufacturer.
Patient Sequence No: 1, Text Type: N, H10


[178203080] On (b)(6) 2018 getinge became aware of an issue with one of surgical lights - blue 80. As it was stated, the locking screw was missing on the spring arm. There was no injury reported however we decided to report the issue in abundance of caution as any parts falling off into sterile field or during procedure could be a source of contamination.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9710055-2019-00344
MDR Report Key9416255
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-12-05
Date of Report2020-03-23
Date Mfgr Received2020-02-27
Date Added to Maude2019-12-05
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 ContactMR. PASCAL JAY
Manufacturer StreetPARC DE LIMERE AVENUE DE LA POMME DE PIN
Manufacturer CityARDON
Manufacturer CountryUS
Manufacturer G1MAQUET SAS
Manufacturer StreetPARC DE LIMERE AVENUE DE LA POMME DE PIN
Manufacturer CityARDON
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBLUE 80
Generic NameLIGHT, SURGICAL, FLOOR STANDING
Product CodeFSS
Date Received2019-12-05
Catalog Number569051999
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMAQUET SAS
Manufacturer AddressPARC DE LIMERE AVENUE DE LA POMME DE PIN ARDON US


Patients

Patient NumberTreatmentOutcomeDate
10 2019-12-05

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