BARD? URETHRAL CATHETERIZATION TRAY WITH RED RUBBER CATHETER 771215

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-17 for BARD? URETHRAL CATHETERIZATION TRAY WITH RED RUBBER CATHETER 771215 manufactured by C.r. Bard, Inc. (covington) -1018233.

Event Text Entries

[142335337] 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


[142335338] It was reported that no urine drained following insertion of the catheter. The staff removed the unknown red rubber foley and attempted to flush it and found that it was obstructed and could not flow. A catheter was inserted and urine drainage was successful.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018233-2019-01988
MDR Report Key8522974
Date Received2019-04-17
Date of Report2019-08-01
Date Mfgr Received2019-07-12
Device Manufacturer Date2018-12-07
Date Added to Maude2019-04-17
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 Report0

Device Details

Brand NameBARD? URETHRAL CATHETERIZATION TRAY WITH RED RUBBER CATHETER
Generic NameCLOSED SYSTEM TRAY
Product CodeEYB
Date Received2019-04-17
Model Number771215
Catalog Number771215
Lot NumberNGCY1043
OperatorHEALTH PROFESSIONAL
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 2019-04-17

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