WRIST RIGHT RADIAL IMPLANT SMALL WARRS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-18 for WRIST RIGHT RADIAL IMPLANT SMALL WARRS manufactured by Stryker Gmbh.

Event Text Entries

[162525866] Device will not be returned. If additional information becomes available, it will be provided in a supplemental report. Device was discarded.
Patient Sequence No: 1, Text Type: N, H10


[162525867] As reported: "demotion wrist removal patient presented to hospital with regard to knee joint pain, investigation revealed chronic wrist pain and possible infection as reported by plastics department. "
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008031020-2019-01288
MDR Report Key9085069
Date Received2019-09-18
Date of Report2019-09-18
Date of Event2019-08-22
Date Mfgr Received2019-08-22
Date Added to Maude2019-09-18
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. KEVIN SMITH
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 NameWRIST RIGHT RADIAL IMPLANT SMALL
Generic NamePROSTHESIS, WRIST, 3 PART METAL-PLASTIC-METAL ARTICULATION, SEMI-CONSTRAINED
Product CodeJWJ
Date Received2019-09-18
Catalog NumberWARRS
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 2019-09-18

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