FDA Adverse Event Malfunction Summary report: N

PRE-FILLED NORMAL SALINE FILLED FLUSH

MDR report key: 3220781 · Received June 28, 2013

Report

Report Number
3220781
Event Type
Malfunction
Date Received
June 28, 2013
Date of Event
June 12, 2013
Report Date
June 28, 2013
Manufacturer
BD MEDICAL SYSTEMS
Product Code
FMF
Product Problem
Yes
Report Source
User Facility report
Reporter Location
IL, US
Reporter Occupation
NURSE

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
295248 PRE-FILLED NORMAL SALINE FILLED FLUSH SYRINGE, PISTON FMF BD MEDICAL SYSTEMS * 301411B

Patients

Seq Age Sex Outcome Treatment
1 *