ECON SCT CTH 14FR VAC BR 1180851147

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 2020-02-07 for ECON SCT CTH 14FR VAC BR 1180851147 manufactured by Covidien.

Event Text Entries

[182429258] 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.
Patient Sequence No: 1, Text Type: N, H10


[182429259] The customer reported the device probe disconnected between the flexible transparent pipe and the rigid green part just before attempting to suck up oral secretions. There was no harm to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9611018-2020-00393
MDR Report Key9681695
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-07
Date of Report2020-02-07
Date of Event2020-01-28
Date Mfgr Received2020-01-28
Date Added to Maude2020-02-07
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 ContactJILL SARAIVA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5086183640
Manufacturer G1COVIDIEN
Manufacturer StreetSRAGH INDUSTRIAL ESTATE, CO, T
Manufacturer CityOFFALY
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameECON SCT CTH 14FR VAC BR
Generic NameCATHETERS, SUCTION, TRACHEOBRONCHIAL
Product CodeBSY
Date Received2020-02-07
Model Number1180851147
Catalog Number1180851147
Lot Number19E152FHX
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressSRAGH INDUSTRIAL ESTATE, CO, T OFFALY EI


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.