OLYMPUS OSF-3 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2000-02-23 for OLYMPUS OSF-3 NA manufactured by Olympus Optical Co., Ltd..

Event Text Entries

[19147573] Complaint description: an olympus sales rep reported that following two recent flexible sigmoidoscopy procedures, two pts had to seek medical treatment for elevated white blood counts.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010047-2000-00010
MDR Report Key265177
Report Source07
Date Received2000-02-23
Date of Report2000-01-27
Date Mfgr Received2000-01-27
Date Added to Maude2000-02-29
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 ContactLAURA STORMS-TYLER
Manufacturer Street2 CORPORATE CENTER DR
Manufacturer CityMELVILLE NY 11747
Manufacturer CountryUS
Manufacturer Postal11747
Manufacturer Phone5168445688
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOLYMPUS
Generic NameSIGMOIDOSCOPE
Product CodeFAM
Date Received2000-02-23
Model NumberOSF-3
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key256719
ManufacturerOLYMPUS OPTICAL CO., LTD.
Manufacturer Address22-2 NISHI-SHINJUKU SHINJUKU-KU, 1-CHOME TOKYO JA 163-91
Baseline Brand NameOLYMPUS
Baseline Generic NameSIGMOIDOSCOPE
Baseline Model NoOSF-3
Baseline Catalog NoNA
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2000-02-23

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