OLYMPUS TELESCOPE WA50013A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2011-11-04 for OLYMPUS TELESCOPE WA50013A manufactured by Olympus Winter & Ibe Gmbh.

Event Text Entries

[2360301] The user facility reported that during a latissimus dorsi (lat) surgery, the users experienced a complete loss of image. The procedure was completed using a different but similar telescope. There was no pt injury reported.
Patient Sequence No: 1, Text Type: D, B5


[9376307] The subject device referenced in this report was returned to olympus for evaluation. The evaluation was able to confirm the user's report of image difficulty. The image was found to be flickering and distorted. There were multiple dents on the outer tube of the telescope, and the optical system lens and distal end cover glass was cracked. The image difficulty was isolated to a damaged r-unit, which was likely damaged due to an impact sustained on the outer tube of the telescope. The device was serviced and returned to the user facility. This report is being submitted as a medical device report in an abundance of caution.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9610773-2011-00033
MDR Report Key2335143
Report Source06
Date Received2011-11-04
Date of Report2011-09-15
Date Mfgr Received2011-10-06
Date Added to Maude2012-03-16
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactLAURA STORMS-TYLER
Manufacturer Street2400 RINGWOOD AVE
Manufacturer CitySAN JOSE CA 95131
Manufacturer CountryUS
Manufacturer Postal95131
Manufacturer Phone4848965688
Manufacturer G1OLYMPUS WINTER & IBE GMBH
Manufacturer StreetKUEHNSTRABE 61
Manufacturer CityHAMBURG 22045
Manufacturer CountryGM
Manufacturer Postal Code22045
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOLYMPUS TELESCOPE
Generic NameTELESCOPE
Product CodeFBP
Date Received2011-11-04
Returned To Mfg2011-10-13
Model NumberWA50013A
Catalog NumberWA50013A
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerOLYMPUS WINTER & IBE GMBH
Manufacturer AddressKUEHNSTRABE 61 HAMBURG 22045 GM 22045


Patients

Patient NumberTreatmentOutcomeDate
10 2011-11-04

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.