S-ROM SHAFT HAMMER SLIDE 531206

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,08 report with the FDA on 2003-06-27 for S-ROM SHAFT HAMMER SLIDE 531206 manufactured by Depuy-raynham, Inc..

Event Text Entries

[275339] Instrument broken at weld. Surgery was delayed for 30 minutes.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2003-00377
MDR Report Key468487
Report Source05,08
Date Received2003-06-27
Date of Report2003-05-28
Date of Event2003-05-28
Date Facility Aware2003-05-28
Report Date2003-05-28
Date Mfgr Received2003-05-28
Date Added to Maude2003-07-01
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 Location3
Manufacturer ContactHANS KUSSEROW, MGR.
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone5743727416
Manufacturer G1DEPUY ORTHOPAEDICS, INC.
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767035
Manufacturer CountryUS
Manufacturer Postal Code02767 0350
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameS-ROM SHAFT HAMMER SLIDE
Generic NameMANUAL SURGICAL INSTRUMENT
Product CodeGFJ
Date Received2003-06-27
Returned To Mfg2003-05-29
Model NumberNA
Catalog Number531206
Lot NumberV0696
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeUNKNOWN
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key457389
ManufacturerDEPUY-RAYNHAM, INC.
Manufacturer Address325 PARAMOUNT DRIVE RAYNAM MA 027670350 US
Baseline Brand NameS-ROM SHAFT HAMMER SLIDE
Baseline Generic NameMALLET, SURGICAL INSTRUMENT
Baseline Model NoNA
Baseline Catalog No531206
Baseline IDNA
Baseline Device FamilyS-RROM SHAFT HAMMER
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2003-06-27

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