FDA Adverse Event Malfunction Summary report: N

1043572-2012-00036

MDR report key: 2669154 · Received July 25, 2012

Report

Report Number
1043572-2012-00036
Event Type
Malfunction
Date Received
July 25, 2012
Date of Event
April 16, 2012
Report Date
January 8, 2026
Manufacturer
STERIS CORPORATION
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown