FDA Adverse Event Injury Summary report: N

TRI TS BASEPLATE SIZE 6

MDR report key: 4090579 · Received September 15, 2014

Report

Report Number
0002249697-2014-03480
Event Type
Injury
Date Received
September 15, 2014
Date of Event
August 25, 2014
Report Date
August 25, 2014
Manufacturer
STRYKER ORTHOPAEDICS-MAHWAH
Product Code
JWH
PMA / PMN Number
K053514
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

DEVICE HISTORY REVIEW: REVIEW OF THE DEVICE HISTORY RECORDS INDICATE DEVICES WERE MANUFACTURED AND ACCEPTED INTO FINAL STOCK WITH NO REPORTED DISCREPANCIES. COMPLAINT HISTORY REVIEW: THERE HAVE BEEN NO OTHER EVENTS REPORTED FOR THE REPORTED MANUFACTURING LOT THE EVENT COULD NOT BE CONFIRMED NOR THE ROOT CAUSE OF THE REPORTED EVENT DETERMINED DUE TO THE MINIMAL INFORMATION RECEIVED. NO FURTHER INVESTIGATION FOR THIS EVENT IS POSSIBLE AT THIS TIME AS NO DEVICES AND INSUFFICIENT INFORMATION WAS RECEIVED BY STRYKER ORTHOPAEDICS. IF DEVICES AND / OR ADDITIONAL INFORMATION BECOME AVAILABLE, THIS INVESTIGATION WILL BE REOPENED.

Additional Manufacturer Narrative · 1

AN EVALUATION OF THE DEVICE CANNOT BE PERFORMED AS THE DEVICE WAS NOT RETURNED TO THE MANUFACTURER DUE TO HOSPITAL POLICY. ADDITIONAL INFORMATION HAS BEEN REQUESTED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE IT WILL BE REPORTED IN A SUPPLEMENTAL REPORT UPON COMPLETION OF THE INVESTIGATION. NOT RETURNED TO THE MANUFACTURER.

Description of Event or Problem · 1

SURGEON COMMENTED ON COLLAPSED MEDIAL FEMORAL CONDYLAR AND POSSIBLE LOOSENING OF FEMUR AND TIBIA COMPONENTS.

Description of Event or Problem · 1

SURGEON COMMENTED ON COLLAPSED MEDIAL FEMORAL CONDYLAR AND POSSIBLE LOOSENING OF FEMUR AND TIBIA COMPONENTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
570469 TRI TS BASEPLATE SIZE 6 IMPLANT JWH STRYKER ORTHOPAEDICS-MAHWAH GNXJ

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention