MAGIC3 GO? INTERMITTENT URINARY CATHETER 53816G

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,other report with the FDA on 2020-02-19 for MAGIC3 GO? INTERMITTENT URINARY CATHETER 53816G manufactured by C.r. Bard, Inc. (covington) -1018233.

Event Text Entries

[183970839] The investigation is still in progress. Once the investigation is complete, a supplemental report will be filed. The device was not returned.
Patient Sequence No: 1, Text Type: N, H10


[183970840] It was reported that the patient experienced discomfort in the urinary tract using the caths sent (53614g). The 53816 was not able to properly hold the lubricant he added (mckesson lube). The packet wasn't large enough to hold it, and stated our pre-lubricated cath "just doesn? T do the trick".
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018233-2020-01159
MDR Report Key9729388
Report SourceCONSUMER,OTHER
Date Received2020-02-19
Date of Report2020-03-10
Date Mfgr Received2020-03-04
Date Added to Maude2020-02-19
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 ContactYONIC ANDERSON
Manufacturer Street8195 INDUSTRIAL BLVD
Manufacturer CityCOVINGTON GA 30014
Manufacturer CountryUS
Manufacturer Postal30014
Manufacturer Phone7707846100
Manufacturer G1C.R. BARD, INC. (COVINGTON) -1018233
Manufacturer Street8195 INDUSTRIAL BLVD
Manufacturer CityCOVINGTON GA 30014
Manufacturer CountryUS
Manufacturer Postal Code30014
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAGIC3 GO? INTERMITTENT URINARY CATHETER
Generic NameMAGIC 3 CATHETER
Product CodeEZD
Date Received2020-02-19
Model Number53816G
Catalog Number53816G
Lot NumberUNK
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerC.R. BARD, INC. (COVINGTON) -1018233
Manufacturer Address8195 INDUSTRIAL BLVD COVINGTON GA 30014 US 30014


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-19

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