FDA Adverse Event Malfunction Summary report: N

6000144-2010-02746

MDR report key: 1992703 · Received February 15, 2011

Report

Report Number
6000144-2010-02746
Event Type
Malfunction
Date Received
February 15, 2011
Report Date
October 15, 2024
Manufacturer
MEDTRONIC MED REL, INC.
PMA / PMN Number
P010031
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention