FDA Adverse Event Malfunction Summary report: N

SAFESNAP SYRINGE

MDR report key: 35088 · Received August 7, 1996

Report

Report Number
MW1009666
Event Type
Malfunction
Date Received
August 7, 1996
Manufacturer
U.S. MEDICAL INSTRUMENTS, INC.
Product Code
FMF
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PT COMPLAINING OF PAIN DUE TO DULL NEEDLES. NEEDLES ALSO SOMETIMES GET LOOSE ON SYRINGE. PLUNGER DOES NOT OPERATE SMOOTHLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SAFESNAP SYRINGE SYRINGE FMF U.S. MEDICAL INSTRUMENTS, INC.

Patients

Seq Age Sex Outcome Treatment
1 NO INFO