N-C CONN TUBE 7MM X3.1M 8888301713

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 2019-03-28 for N-C CONN TUBE 7MM X3.1M 8888301713 manufactured by Covidien.

Event Text Entries

[140275245] Additional information has been requested but to date has not been received. 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


[140275246] The customer reports that the blue tip came off from the suction manifold and there was no suction possible. There was medical intervention required.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9612030-2019-02132
MDR Report Key8461948
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-03-28
Date of Report2019-07-01
Date of Event2019-02-27
Date Mfgr Received2019-03-01
Date Added to Maude2019-03-28
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 StreetCALLE 9 SUR NO. 125 CUIDAD IND
Manufacturer CityTIJUANA 22500
Manufacturer CountryMX
Manufacturer Postal Code22500
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameN-C CONN TUBE 7MM X3.1M
Generic NameTUBING, NONINVASIVE
Product CodeGAZ
Date Received2019-03-28
Model Number8888301713
Catalog Number8888301713
Lot Number1727617564
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressCALLE 9 SUR NO. 125 CUIDAD IND TIJUANA 22500 MX 22500


Patients

Patient NumberTreatmentOutcomeDate
10 2019-03-28

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