FDA Adverse Event Injury Summary report: N

TRIDENT X3 ECCENTRIC 0° 32MM ID

MDR report key: 3984390 · Received August 6, 2014

Report

Report Number
0002249697-2014-03042
Event Type
Injury
Date Received
August 6, 2014
Date of Event
July 21, 2014
Report Date
July 21, 2014
Manufacturer
STRYKER ORTHOPAEDICS-MAHWAH
Product Code
LPH
PMA / PMN Number
K033716
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

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

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.

Description of Event or Problem · 1

PATIENT PRESENTED WITH A DISLOCATED HIP. DOCTOR REMOVED THE LINER AND PUT IN A CONSTRAINED LINER.

Description of Event or Problem · 1

PER SALES REP FIRST RESPONSE THE SUBJECT DEVICE WAS USED IN CONJUNCTION WITH A COMPETITOR FEMORAL HEAD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
461939 TRIDENT X3 ECCENTRIC 0° 32MM ID IMPLANT LPH STRYKER ORTHOPAEDICS-MAHWAH 14KAY

Patients

Seq Age Sex Outcome Treatment
1 60 YR Required Intervention