FDA Adverse Event Malfunction Summary report: N

3005075853-2010-05501

MDR report key: 1923946 · Received December 14, 2010

Report

Report Number
3005075853-2010-05501
Event Type
Malfunction
Date Received
December 14, 2010
Date of Event
August 13, 2010
Report Date
May 15, 2024
Manufacturer
ETHICON ENDO-SURGERY, LLC.
PMA / PMN Number
K051002
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown