ARGYLE 5558301726

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2017-07-18 for ARGYLE 5558301726 manufactured by Covidien.

Event Text Entries

[80281805] Submit date: 07/18/17. An investigation is currently under way; upon completion the results will be forwarded. A good faith effort will be made to obtain the applicable information relevant to the report. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[80281806] The customer states the 7 mm suction tubing in the total knee pack is kinked and causing issue with the suction flow. The kink appears on one end and not the other end.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9612030-2017-05124
MDR Report Key6721048
Report SourceDISTRIBUTOR,FOREIGN
Date Received2017-07-18
Date of Report2018-01-10
Date of Event2017-06-13
Date Mfgr Received2017-06-20
Date Added to Maude2017-07-18
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 ContactEDWARD ALMEIDA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524151
Manufacturer G1COVIDIEN
Manufacturer StreetCALLE 9 SUR NO. 125 CUIDAD
Manufacturer CityTIJUANA,NA 92173
Manufacturer CountryMX
Manufacturer Postal Code92173
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARGYLE
Generic NameTUBING, NONINVASIVE
Product CodeGAZ
Date Received2017-07-18
Model Number5558301726
Catalog Number5558301726
Lot Number706515164X
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressCALLE 9 SUR NO. 125 CUIDAD TIJUANA,NA 92173 MX 92173


Patients

Patient NumberTreatmentOutcomeDate
10 2017-07-18

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