FDA Adverse Event Malfunction Summary report: N

BD 60ML LUER-LOK SYRINGE

MDR report key: 6016813 · Received October 7, 2016

Report

Report Number
MW5065264
Event Type
Malfunction
Date Received
October 7, 2016
Date of Event
October 6, 2016
Report Date
October 6, 2016
Manufacturer
BD
Product Code
FPA
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

SYRINGE FLUID LEAKAGE WHEN PREPARING CHEMOTHERAPY. LEAK EXTENDED PAST THE FIRST AND SECOND RIB ON THE BLACK STOPPER ON THE PARENTERAL SYRINGE PLUNGER ROD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
662465 BD 60ML LUER-LOK SYRINGE SYRINGE FPA BD 6193998

Patients

Seq Age Sex Outcome Treatment
1