UNKNOWN SMART TOE IMPLANT UNK_SEL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-10-18 for UNKNOWN SMART TOE IMPLANT UNK_SEL manufactured by Stryker Gmbh.

Event Text Entries

[57778741] Device will not be returned. If additional information becomes available it will be provided on a supplemental report. Device will not be returned.
Patient Sequence No: 1, Text Type: N, H10


[57778742] Per the patient, in 2015 they inserted a smart toe into the 3rd toe; it broke. In 2016 they removed the broken implant from the 3rd toe and replaced it with a wire.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008031020-2016-00512
MDR Report Key6038589
Date Received2016-10-18
Date of Report2016-09-20
Date of Event2016-06-01
Date Mfgr Received2016-09-20
Date Added to Maude2016-10-18
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 Location3
Manufacturer ContactMR. ROSE HAAS
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2018315000
Manufacturer G1STRYKER GMBH
Manufacturer StreetBOHNACKERWEG 1 POSTFACH
Manufacturer CitySELZACH 2545
Manufacturer CountryCH
Manufacturer Postal Code2545
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameUNKNOWN SMART TOE IMPLANT
Generic NameIMPLANT
Product CodeKWD
Date Received2016-10-18
Catalog NumberUNK_SEL
Lot NumberUNKNOWN
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER GMBH
Manufacturer AddressBOHNACKERWEG 1 POSTFACH SELZACH 2545 CH 2545


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-10-18

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