PORTEX ANAESTHESIA BREATHING CIRCUIT, SINGLE-USE C45091795D-NL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-16 for PORTEX ANAESTHESIA BREATHING CIRCUIT, SINGLE-USE C45091795D-NL manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[183476537] Information was received that a smiths medical portex anaesthesia breathing circuit, single-use during procedures the bushing and the bag coming disconnected, no adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02019
MDR Report Key9833531
Report SourceUSER FACILITY
Date Received2020-03-16
Date of Report2020-03-15
Date Mfgr Received2020-02-14
Date Added to Maude2020-03-16
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 ContactDAVE HALVERSON
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer G1SMITHS MEDICAL INTERNATIONAL LTD
Manufacturer StreetBOUNDARY ROAD
Manufacturer CityHYTHE, CT216JL
Manufacturer CountryUK
Manufacturer Postal CodeCT21 6JL
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePORTEX ANAESTHESIA BREATHING CIRCUIT, SINGLE-USE
Generic NameANESTHESIA BREATHING CIRCUIT KIT (ADULT & PEDIATRIC) PRODUCT CODE: OFP
Product CodeOFP
Date Received2020-03-16
Returned To Mfg2020-02-28
Catalog NumberC45091795D-NL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-16

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