UNKNOWN SCORPIO PS INSERT SIZE 7 8MM UNK_REC

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other report with the FDA on 2017-02-03 for UNKNOWN SCORPIO PS INSERT SIZE 7 8MM UNK_REC manufactured by Stryker Orthopaedics-mahwah.

Event Text Entries

[66523196] It was noted that the device is not available for evaluation. Additional information has been requested. Should additional information become available, it will be provided in a supplemental report upon completion of the investigation.
Patient Sequence No: 1, Text Type: N, H10


[66523197] Patient had left total knee revision with a liner exchange.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0002249697-2017-00460
MDR Report Key6301448
Report SourceHEALTH PROFESSIONAL,OTHER
Date Received2017-02-03
Date of Report2017-02-03
Date of Event2017-01-10
Date Mfgr Received2017-01-10
Date Added to Maude2017-02-03
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 ContactMS. SARAH SMELKO
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2018315000
Manufacturer G1STRYKER ORTHOPAEDICS-MAHWAH
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal Code07430
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN SCORPIO PS INSERT SIZE 7 8MM
Generic NameKNEE IMPLANT
Product CodeHSH
Date Received2017-02-03
Catalog NumberUNK_REC
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ORTHOPAEDICS-MAHWAH
Manufacturer Address325 CORPORATE DRIVE MAHWAH NJ 07430 US 07430


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2017-02-03

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