AIRLIFE SOFT LARIAT CUSHION CANNULA SFT2600

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-03-13 for AIRLIFE SOFT LARIAT CUSHION CANNULA SFT2600 manufactured by Carefusion.

Event Text Entries

[69758792]
Patient Sequence No: 1, Text Type: N, H10


[69758793] In the supply closet, staff found unused airlife adult cushion nasal cannulas in closed packages with white residue all over the tubing.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6398660
MDR Report Key6398660
Date Received2017-03-13
Date of Report2017-03-02
Date of Event2017-02-09
Report Date2017-03-02
Date Reported to FDA2017-03-02
Date Reported to Mfgr2017-03-02
Date Added to Maude2017-03-13
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAIRLIFE SOFT LARIAT CUSHION CANNULA
Generic NameOXYGEN ADMINISTRATION KIT
Product CodeOGL
Date Received2017-03-13
Returned To Mfg2017-02-21
Catalog NumberSFT2600
Lot Number0000882081
Device AvailabilityR
Device Age0 YR
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCAREFUSION
Manufacturer Address400 EAST FOSTER RD MANNFORD OK 74044 US 74044


Patients

Patient NumberTreatmentOutcomeDate
10 2017-03-13

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