CODMAN DISPOSABLES PERFORATOR 26-1221

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2004-05-11 for CODMAN DISPOSABLES PERFORATOR 26-1221 manufactured by Codman & Shurtleff, Inc..

MAUDE Entry Details

Report Number1226348-2004-00140
MDR Report Key559592
Report Source05,06
Date Received2004-05-11
Date of Report2004-04-14
Date of Event2004-04-14
Date Mfgr Received2004-04-14
Device Manufacturer Date2004-03-01
Date Added to Maude2004-12-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag0
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional0
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactMATTHEW KING
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal02767
Manufacturer Phone5088283106
Manufacturer G1CODMAN & SHURTLEFF, INC.
Manufacturer StreetNEW BEDFORD INDUSTRIAL PARK
Manufacturer CityNEW BEDFORD MA 02745
Manufacturer CountryUS
Manufacturer Postal Code02745
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameCODMAN DISPOSABLES PERFORATOR
Generic NameDRILLS, BURRS, TREPHINES & ACCESSORIES
Product CodeKAT
Date Received2004-05-11
Returned To Mfg2004-04-28
Model NumberNA
Catalog Number26-1221
Lot NumberCW820
Device Expiration Date2009-03-31
Device AvailabilityR
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key514936
ManufacturerCODMAN & SHURTLEFF, INC.
Manufacturer AddressNEW BEDFORD INDUSTRIAL PARK NEW BEDFORD MA 02745 US
Baseline Brand NameCODMAN DISPOSABLE PERFORATOR
Baseline Generic NameCOMPOUND DRILL
Baseline Model NoNA
Baseline Catalog No26-1221
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2004-05-11

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