FDA Adverse Event Injury Summary report: N

PERFECTA(R) SLT TAPER COLLARED HIP STEM

MDR report key: 2895561 · Received January 3, 2013

Report

Report Number
1043534-2013-00012
Event Type
Injury
Date Received
January 3, 2013
Date of Event
December 1, 2010
Report Date
December 10, 2012
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
Product Code
LPH
PMA / PMN Number
K883618
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION IS NOT COMPLETE. TRENDS WILL BE EVALUATED. THE EVENT CODE IS ADDRESSED IN THE PACKAGE INSERT. THIS REPORT WILL BE UPDATED WHEN THE INVESTIGATION IS COMPLETE. THIS IS THE SAME EVENT AS 1043534-2013-00013, 00014.

Additional Manufacturer Narrative · 1

CONCLUSION: NO CONCLUSION CAN BE DRAWN.THE COMPLAINT WAS REVIEWED AND ANALYSIS SHOWED NO TREND FOR ITEM/LOT. THE PACKAGE INSERT WAS ALSO REVIEWED. THE PRODUCT WAS NOT RETURNED.EVIDENCE THAT PRODUCT IN SPECIFICATION WHEN USED.(B)(4)

Description of Event or Problem · 1

ALLEGEDLY REVISED DUE TO MOM COMPLICATIONS. RIGHT HIP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2786 PERFECTA(R) SLT TAPER COLLARED HIP STEM HIP COMPONENT, CODE:LPH LPH WRIGHT MEDICAL TECHNOLOGY, INC. 03478330

Patients

Seq Age Sex Outcome Treatment
1 71 YR Required Intervention