FDA Adverse Event Malfunction Summary report: N

3005075853-2010-05417

MDR report key: 1880525 · Received October 22, 2010

Report

Report Number
3005075853-2010-05417
Event Type
Malfunction
Date Received
October 22, 2010
Date of Event
August 26, 2010
Report Date
May 15, 2024
Manufacturer
ETHICON ENDO-SURGERY, LLC.
PMA / PMN Number
K820837
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TW
Reporter Occupation
OTHER

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown