SMART STAPES PISTON * UNK

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 2006-11-22 for SMART STAPES PISTON * UNK manufactured by Gyrus Ent.

Event Text Entries

[15187498] Reportedly a patient required a revision surgery following a stapes replacement with a smart piston. The report indicates that the patient may have a nickel sensitivity. No device malfunction claim has been made. Three attempts at obtaining further information have been made with no success. No product has been returned to gyrus ent for evaluation. Nickel sensitivity is a known contraindication for the smart piston.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1037007-2006-00003
MDR Report Key794881
Report Source05,06
Date Received2006-11-22
Date of Report2006-11-22
Date Mfgr Received2006-10-25
Date Added to Maude2006-12-18
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 FDA3
Event Location0
Manufacturer ContactMR. DOLAN MILLS
Manufacturer Street2925 APPLING RD
Manufacturer CityBARTLETT TN 38133
Manufacturer CountryUS
Manufacturer Postal38133
Manufacturer Phone9013730200
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSMART STAPES PISTON
Generic NamePORP
Product CodeETB
Date Received2006-11-22
Model Number*
Catalog NumberUNK
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagY
Date Removed*
Device Sequence No1
Device Event Key782499
ManufacturerGYRUS ENT
Manufacturer Address* BARTLETT TN 38133 US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2006-11-22

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