DRAINBAG W/RFLX VLV, SAMPLPOR DYNC1654 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2001-04-13 for DRAINBAG W/RFLX VLV, SAMPLPOR DYNC1654 * manufactured by Medline Industries, Inc..

Event Text Entries

[21593190] Reportedly, the fluid is backing up in the tubing and gave the user an urinary tract infection.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1417592-2001-00008
MDR Report Key327654
Report Source05,07
Date Received2001-04-13
Date of Report2001-04-12
Date Facility Aware2001-03-29
Date Added to Maude2001-04-20
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactSTACEY BOLEN
Manufacturer StreetONE MEDLINE PLACE
Manufacturer CityMUNDELEIN IL 60060
Manufacturer CountryUS
Manufacturer Postal60060
Manufacturer Phone8478372843
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDRAINBAG W/RFLX VLV, SAMPLPOR
Generic Name*
Product CodeEYZ
Date Received2001-04-13
Model NumberDYNC1654
Catalog Number*
Lot Number1A3007
ID Number*
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedU
Device Sequence No1
Device Event Key317035
ManufacturerMEDLINE INDUSTRIES, INC.
Manufacturer AddressONE MEDLINE PL. MUNDELEIN IL 60060 US
Baseline Brand Name@ DRAINBAG W/RFLX VLV, SAMPLPOR
Baseline Generic NameURINE COLLECTOR
Baseline Model NoDYNC1654
Baseline Device FamilyDN11
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 2001-04-13

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