NELLCOR D-YS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-04-05 for NELLCOR D-YS manufactured by Nellcor.

Event Text Entries

[41939520] (b)(4). The customer did not retain the lot number. The date of manufacture cannot be determined.
Patient Sequence No: 1, Text Type: N, H10


[41939521] The customer reported low saturation readings. This led to hospitalizing a child while the patient was fine.
Patient Sequence No: 1, Text Type: D, B5


[47302416] (b)(4). Low readings could not be duplicated. There was no fault found with the sensor.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2936999-2016-00255
MDR Report Key5549010
Date Received2016-04-05
Date of Report2016-03-11
Date of Event2016-03-11
Date Mfgr Received2016-03-11
Date Added to Maude2016-04-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactTHOM MCNAMARA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524811
Manufacturer G1COVIDIEN
Manufacturer StreetBLVD. INSURGENTES PARCELA #37
Manufacturer CityTIJUANA, BC
Manufacturer CountryMX
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNELLCOR
Generic NameDURA-Y SENSOR
Product CodeDPZ
Date Received2016-04-05
Model NumberD-YS
Catalog NumberD-YS
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNELLCOR
Manufacturer AddressBLVD. INSURGENTES PARCELA #37 TIJUANA, BC MX


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-04-05

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