ALPINE RESUABLE LB LATEX 32 OZ ST 5596001400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2010-09-20 for ALPINE RESUABLE LB LATEX 32 OZ ST 5596001400 manufactured by Coloplast Manufacturing Us, Llc.

Event Text Entries

[1372395] Patient identifier: (b)(6). Date of event: best estimate is (b)(6) 2010. According to the information received, the end user states that the anti reflux was not working. Patient has used this type of bag many years but the first time using this bag urine would not go into the bag. No unused bag to return.
Patient Sequence No: 1, Text Type: D, B5


[8701984] The product was not available to be returned. Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurence. Should the device or additional information be received, a follow up report will be filed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2183558-2010-00036
MDR Report Key1839084
Report Source04
Date Received2010-09-20
Date of Report2010-08-24
Date Mfgr Received2010-08-24
Date Added to Maude2012-01-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMR. BRIAN SCHMIDT
Manufacturer Street1601 WEST RIVER ROAD NORTH
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal55411
Manufacturer Phone6123024987
Manufacturer G1COLOPLAST MANUFACTURING US, LLC
Manufacturer Street1185 WILLOW LAKE BLVD
Manufacturer CityVADNAIS HEIGHTS, MN 55110 55110
Manufacturer CountryUS
Manufacturer Postal Code55110
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameALPINE RESUABLE LB LATEX 32 OZ ST
Generic NameURINE LEG BAG
Product CodeNNW
Date Received2010-09-20
Model Number5596001400
Catalog Number5596001400
Lot NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOLOPLAST MANUFACTURING US, LLC
Manufacturer Address1185 WILLOW LAKE BLVD. VADNAIS HEIGHTS MN 55110 US 55110


Patients

Patient NumberTreatmentOutcomeDate
10 2010-09-20

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