CAREONE UPC#341520317170 766353

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2019-06-07 for CAREONE UPC#341520317170 766353 manufactured by Aso Llc.

MAUDE Entry Details

Report Number1038758-2019-00015
MDR Report Key8680732
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2019-06-07
Date of Report2019-03-18
Date of Event2019-03-18
Date Mfgr Received2019-03-18
Device Manufacturer Date2018-07-17
Date Added to Maude2019-06-07
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. FEDERICO JULIAO
Manufacturer Street300 SARASOTA CENTER BLVD.
Manufacturer CitySARASOTA FL 34240
Manufacturer CountryUS
Manufacturer Postal34240
Manufacturer G1ASO LLC
Manufacturer Street300 SARASOTA CENTER BLVD.
Manufacturer CitySARASOTA FL 34240
Manufacturer CountryUS
Manufacturer Postal Code34240
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCAREONE
Generic NameDRUG FREE NASAL STRIPS REGULAR STRENGTH TAN LARGE
Product CodeLWF
Date Received2019-06-07
Model NumberUPC#341520317170
Catalog Number766353
Lot Number00088268
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerASO LLC
Manufacturer Address300 SARASOTA CENTER BLVD. SARASOTA FL 34240 US 34240


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-06-07

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