VAPRO HYDROPHILIC IC CH14 16 IN COUDE 73144

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-01-22 for VAPRO HYDROPHILIC IC CH14 16 IN COUDE 73144 manufactured by Hollister Incorporated.

MAUDE Entry Details

Report Number9616668-2020-00002
MDR Report Key9616253
Report SourceCONSUMER
Date Received2020-01-22
Date of Report2020-01-22
Date of Event2019-12-30
Date Mfgr Received2019-12-30
Device Manufacturer Date2019-04-17
Date Added to Maude2020-01-22
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. LINDA WISOWATY
Manufacturer Street2000 HOLLISTER DRIVE
Manufacturer CityLIBERTYVILLE IL 600483781
Manufacturer CountryUS
Manufacturer Postal600483781
Manufacturer Phone8476802170
Manufacturer G1HOLLISTER ULC
Manufacturer StreetFOXFORD RD. REHINS
Manufacturer CityBALLINA,
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVAPRO HYDROPHILIC IC CH14 16 IN COUDE
Generic NameVAPRO HYDROPHILIC IC CH14 16 IN COUDE
Product CodeGBM
Date Received2020-01-22
Returned To Mfg2020-01-16
Catalog Number73144
Lot Number9C313
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerHOLLISTER INCORPORATED
Manufacturer Address2000 HOLLISTER DRIVE LIBERTYVILLE. 600483781 US 600483781


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-22

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