SPT-05172 IN CARDIAC CATH PACK DYNJV0193B *

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 2002-11-05 for SPT-05172 IN CARDIAC CATH PACK DYNJV0193B * manufactured by Medline Industries, Inc..

Event Text Entries

[256445] Reportedly the tips of the hemostat were sharp and an artery on a patient was allegedly punctured. Pressure was applied to the site and no further medical treatment was required.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1423395-2002-00005
MDR Report Key426790
Report Source05,07
Date Received2002-11-05
Date of Report2002-11-05
Date of Event2002-10-07
Date Mfgr Received2002-10-07
Device Manufacturer Date2002-06-01
Date Added to Maude2002-11-13
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 ContactANDREA HAFERKAMP
Manufacturer StreetONE MEDLINE PLACE
Manufacturer CityMUNDELEIN IL 60060
Manufacturer CountryUS
Manufacturer Postal60060
Manufacturer Phone8478372759
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSPT-05172 IN CARDIAC CATH PACK
Generic NameHEMOSTAT FORCEPS IN CARDIAC CATH PACK
Product CodeHRQ
Date Received2002-11-05
Returned To Mfg2002-10-08
Model NumberDYNJV0193B
Catalog Number*
Lot Number02FD1953
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key415815
ManufacturerMEDLINE INDUSTRIES, INC.
Manufacturer AddressONE MEDLINE PLACE MUNDELEIN IL 60060 US
Baseline Brand NameHEMOSTAT FORCEPS IN CARDIAC CATH PACK
Baseline Model NoDYNJV0193B
Baseline Device FamilyPROV
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2002-11-05

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