BLUELINE ARD567911211C

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 2020-02-21 for BLUELINE ARD567911211C manufactured by Maquet Sas.

Event Text Entries

[181999851] Additional information will be provided upon results of investigation. Device not returned to manufacturer.
Patient Sequence No: 1, Text Type: N, H10


[181999852] On (b)(6) 2020 getinge became aware of an issue with one of our surgical light? Blue. As it was stated by the customer during the procedure part of the device has fallen down and additionally deformation of the device occurred due to overheating of the device. No injury was reported due to mentioned issue, however we decided to report this case in abundance of caution as any parts falling down might cause contamination or led to serious injury. Manufacturer's reference number: (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9710055-2020-00023
MDR Report Key9738886
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-21
Date of Report2020-04-03
Date of Event2020-02-12
Date Mfgr Received2020-03-10
Device Manufacturer Date2009-01-31
Date Added to Maude2020-02-21
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 NameBLUELINE
Generic NameLIGHT, SURGICAL, CEILING MOUNTED
Product CodeFSY
Date Received2020-02-21
Model NumberARD567911211C
Catalog NumberARD567911211C
OperatorHEALTH PROFESSIONAL
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 2020-02-21

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