ARGYLE 8888750018

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-06-21 for ARGYLE 8888750018 manufactured by Covidien.

Event Text Entries

[78235472]
Patient Sequence No: 1, Text Type: N, H10


[78235473] The customer states that 9 units arrived with kinked tubing.
Patient Sequence No: 1, Text Type: D, B5


[135209175] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1282497-2017-05183
MDR Report Key6657015
Date Received2017-06-21
Date of Report2018-10-05
Date of Event2017-05-30
Date Mfgr Received2018-08-08
Date Added to Maude2017-06-21
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 ContactEDWARD ALMEIDA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524151
Manufacturer G1COVIDIEN
Manufacturer StreetBOULEVARD INSURGENTES 19030
Manufacturer CityTIJUANA 22225
Manufacturer CountryMX
Manufacturer Postal Code22225
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameARGYLE
Generic NameCATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION
Product CodeKDH
Date Received2017-06-21
Model Number8888750018
Catalog Number8888750018
Lot Number170620003
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressBOULEVARD INSURGENTES 19030 TIJUANA 22225 MX 22225


Patients

Patient NumberTreatmentOutcomeDate
10 2017-06-21

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