REBREATHING BAG 2707202

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2003-03-21 for REBREATHING BAG 2707202 manufactured by Rusch Manufacturing (uk).

Event Text Entries

[265587] Customer reports bag ripped during use.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010092-2003-00038
MDR Report Key450690
Report Source06
Date Received2003-03-21
Date of Report2003-03-14
Date Mfgr Received2003-03-11
Date Added to Maude2003-04-01
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 Location0
Manufacturer ContactROLANDA SCOTT, COORDINATOR
Manufacturer Street2450 MEADOWBROOK PARKWAY
Manufacturer CityDULUTH GA 30136
Manufacturer CountryUS
Manufacturer Postal30136
Manufacturer Phone7706230816
Manufacturer G1RUSCH, INC.
Manufacturer Street2450 MEADOWBROOK PARKWAY
Manufacturer CityDULUTH GA 30136
Manufacturer CountryUS
Manufacturer Postal Code30136
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameREBREATHING BAG
Generic NameANESTHESIA
Product CodeBYW
Date Received2003-03-21
Model NumberNA
Catalog Number2707202
Lot NumberUNK
ID NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key439683
ManufacturerRUSCH MANUFACTURING (UK)
Manufacturer AddressPORTADOWN RD., LURGAN CRAIGAVON CO. ARMAGH, N. IRELAND UK BT66 8RD
Baseline Brand NameREBREATHING BAG
Baseline Generic NameANESTHESIA
Baseline Model NoNA
Baseline Catalog No2707202
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2003-03-21

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