FDA Adverse Event Malfunction Summary report: N

SYRINGE TIP

MDR report key: 2875444 · Received December 7, 2012

Report

Report Number
MW5028087
Event Type
Malfunction
Date Received
December 7, 2012
Report Date
December 7, 2012
Manufacturer
BD
Product Code
FMF
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

PHASEAL SYRINGE TIP LEAKED AT JUNCTION FURTHEST FROM SYRINGE. PT RECEIVED ADEQUATE DRUG. NURSE AND PT WERE NOT EXPOSED. NURSE DONNED APPROPRIATE CLOTHING AND PATIENT WAS NOT PHYSICALLY EXPOSED. DATE OF USE: (B)(6) 2012. REASON FOR USE: SCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SYRINGE TIP SYRINGE TIP FMF BD

Patients

Seq Age Sex Outcome Treatment
1