PORTEX ? FIRST BREATH ADULT TRACHEOSTOMY MASK 001305

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-12-22 for PORTEX ? FIRST BREATH ADULT TRACHEOSTOMY MASK 001305 manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[63483462] Customer has not yet returned the device to the manufacturer for device evaluation. When and if the device becomes available and is returned and evaluated the manufacturer will file a follow-up report detailing the results of the evaluation. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[63483463] It was reported that the patient experienced pressure wounds from the tracheostomy mask since the product material has changed to a more solid material. It is unknown whether the event has been resolved, however, it was reported that the patient was changed to a competitor's brand. No further adverse health outcomes have been reported. See mfr: 3012307300-2016-00595.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2016-00593
MDR Report Key6200910
Date Received2016-12-22
Date of Report2016-12-01
Date Mfgr Received2016-12-01
Date Added to Maude2016-12-22
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 ContactMS. LISA PERZ
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone7633833074
Manufacturer G1SMITHS MEDICAL NORTH AMERICA
Manufacturer Street9124 POLK LANE SUITE 101
Manufacturer CityOLIVE BRANCH MS 38654
Manufacturer CountryUS
Manufacturer Postal Code38654
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePORTEX ? FIRST BREATH ADULT TRACHEOSTOMY MASK
Generic NameMASK, OXYGEN, NON-REBREATHING
Product CodeKGB
Date Received2016-12-22
Catalog Number001305
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS MN 55442 US 55442


Patients

Patient NumberTreatmentOutcomeDate
10 2016-12-22

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