MALLINCKRODT 107-75

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2019-12-26 for MALLINCKRODT 107-75 manufactured by Mallinckrodt Medical.

Event Text Entries

[173784097] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[173784098] According to the reporter, post operatively, the device had air leakage on the cuff. The patient required reintubation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8040459-2019-00127
MDR Report Key9521648
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2019-12-26
Date of Report2019-12-26
Date of Event2019-11-11
Date Mfgr Received2019-12-12
Date Added to Maude2019-12-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactAVI KLUGER
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone3035306582
Manufacturer G1MALLINCKRODT MEDICAL
Manufacturer StreetCORNAMADDY
Manufacturer CityATHLONE 3810
Manufacturer Postal Code3810
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMALLINCKRODT
Generic NameAIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
Product CodeCAE
Date Received2019-12-26
Model Number107-75
Catalog Number107-75
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMALLINCKRODT MEDICAL
Manufacturer AddressCORNAMADDY ATHLONE 3810 3810


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-12-26

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