FDA Adverse Event Malfunction Summary report: N

BD 3 ML SYRINGE LUER-LOK TIP

MDR report key: 10431250 · Received August 19, 2020

Report

Report Number
MW5096155
Event Type
Malfunction
Date Received
August 19, 2020
Date of Event
August 18, 2020
Report Date
August 18, 2020
Manufacturer
BECTON DICKINSON AND COMPANY
Product Code
FMF
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
VA, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

BD 3 ML LUER-LOK TIP SYRINGE, LOT 0150246 DOES NOT HAVE ANY INK ON THE SYRINGES TO MARK THE MEASUREMENTS. SOME NURSES REPORTED FINDING THESE SEALED UNMARKED SYRINGES IN PREVIOUS DAYS. SIXTY ONE SYRINGES WERE REMAINING IN OUR FLOOR STOCK THAT HAD THIS DEFECT. THEY HAVE BEEN REMOVED FROM THE FLOOR STOCK AND OUR SUPPLY MANAGER NOTIFIED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
889422 BD 3 ML SYRINGE LUER-LOK TIP SYRINGE, PISTON FMF BECTON DICKINSON AND COMPANY 0150246

Patients

Seq Age Sex Outcome Treatment
1