FDA Adverse Event Malfunction Summary report: N

1043534-2012-00513

MDR report key: 2787596 · Received October 15, 2012

Report

Report Number
1043534-2012-00513
Event Type
Malfunction
Date Received
October 15, 2012
Date of Event
October 14, 2011
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ND, US
Reporter Occupation
OTHER
Health Professional
N

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown