ARGYLE 8884729500

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-04 for ARGYLE 8884729500 manufactured by Covidien.

Event Text Entries

[123200442] The incident sample has been requested but to date has not been received for evaluation. If the sample is received, or if additional information pertinent to the incident is obtained, a follow-up report will be submitted. As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[123200443] The customer reported that he noticed during initial inspection prior to use, one tube is kinked.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9611018-2018-00013
MDR Report Key7934321
Date Received2018-10-04
Date of Report2018-11-28
Date of Event2018-09-26
Date Mfgr Received2018-10-25
Device Manufacturer Date2018-01-29
Date Added to Maude2018-10-04
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 StreetSRAGH INDUSTRIAL ESTATE,RAHAN
Manufacturer CityTULLAMORE
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameARGYLE
Generic NameTUBE, ASPIRATING, FLEXIBLE, CONNECTING
Product CodeBYY
Date Received2018-10-04
Returned To Mfg2018-10-08
Model Number8884729500
Catalog Number8884729500
Lot Number18A026FHX
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressSRAGH INDUSTRIAL ESTATE,RAHAN TULLAMORE


Patients

Patient NumberTreatmentOutcomeDate
10 2018-10-04

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