FDA Adverse Event Malfunction Summary report: N

LUER-LOK SYRINGE

MDR report key: 22637 · Received June 21, 1995

Report

Report Number
MW1006303
Event Type
Malfunction
Date Received
June 21, 1995
Date of Event
June 13, 1995
Report Date
June 13, 1995
Manufacturer
BECTON DICKINSON & CO.
Product Code
FMF
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MD, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

REMOVED SYRINGE FROM STERILE WRAPPER INSIDE OF HOOD AND FOUND WHAT LOOKS LIKE MUD ON THE OUTSIDE OF THE SYRINGE. (SUSPECTED CONTAMINATION).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LUER-LOK SYRINGE 5ML SYRINGE FMF BECTON DICKINSON & CO.

Patients

Seq Age Sex Outcome Treatment
1 *