INVACARE PLATINUM 10 OXYGEN CONCENTRATOR IRC10LXO2

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2019-11-25 for INVACARE PLATINUM 10 OXYGEN CONCENTRATOR IRC10LXO2 manufactured by Invacare Florida.

MAUDE Entry Details

Report Number1031452-2019-00107
MDR Report Key9370522
Report SourceOTHER
Date Received2019-11-25
Date of Report2019-11-01
Date of Event2019-10-22
Date Mfgr Received2019-11-01
Device Manufacturer Date2010-10-01
Date Added to Maude2019-11-25
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 ContactMR. JASON FIEST
Manufacturer StreetONE INVACARE WAY
Manufacturer CityELYRIA OH 44035
Manufacturer CountryUS
Manufacturer Postal44035
Manufacturer Phone8003336900
Manufacturer G1INVACARE FLORIDA
Manufacturer Street2101 EAST LAKE MARY BLVD
Manufacturer CitySANFORD FL 32773
Manufacturer CountryUS
Manufacturer Postal Code32773
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINVACARE PLATINUM 10 OXYGEN CONCENTRATOR
Generic NameGENERATOR, OXYGEN, PORTABLE
Product CodeCAW
Date Received2019-11-25
Model NumberIRC10LXO2
Catalog NumberIRC10LXO2
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINVACARE FLORIDA
Manufacturer Address2101 EAST LAKE MARY BLVD SANFORD FL 32773 US 32773


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-25

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