BLUE NEOPRENE BAG 3L 78300APEX

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2002-09-16 for BLUE NEOPRENE BAG 3L 78300APEX manufactured by Rusch Inc. Manufacturing (uk).

Event Text Entries

[15484867] Bag burst.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010092-2002-00189
MDR Report Key418220
Report Source08
Date Received2002-09-16
Date of Report2002-09-12
Date Mfgr Received2002-09-12
Date Added to Maude2002-09-26
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 ContactROLANDA SCOTT, DOCUMENT CONTROL
Manufacturer Street2450 MEADOWBROOK PARKWAY
Manufacturer CityDULUTH GA 30136
Manufacturer CountryUS
Manufacturer Postal30136
Manufacturer Phone7706230816
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBLUE NEOPRENE BAG 3L
Generic NameANESTHESIA
Product CodeBYW
Date Received2002-09-16
Model NumberNA
Catalog Number78300APEX
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key407256
ManufacturerRUSCH INC. MANUFACTURING (UK)
Manufacturer AddressPORTADOWN RD., LURGAN CRAIGAVON CO. ARMAGH, N. IRELAND UK BT66 8RD
Baseline Brand NameBLUE NEOPRENE BAG
Baseline Generic NameNA
Baseline Model NoNA
Baseline Catalog No78300APEX
Baseline IDNA
Baseline Device FamilyENTERAL
Baseline Shelf Life ContainedN
Baseline Shelf Life [Months]*
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 2002-09-16

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