FDA Adverse Event Injury Summary report: N

2242816-2011-00501

MDR report key: 2221491 · Received August 24, 2011

Report

Report Number
2242816-2011-00501
Event Type
Injury
Date Received
August 24, 2011
Manufacturer
EBI, LLC
Adverse Event
Yes
Report Source
Manufacturer report

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown