FDA Adverse Event Other Summary report: N

BD ORAL AMBER SYRINGE 1 ML

MDR report key: 1310546 · Received February 9, 2009

Report

Report Number
MW5009929
Event Type
Other
Date Received
February 9, 2009
Date of Event
February 1, 2009
Report Date
February 9, 2009
Product Code
KYX
Report Source
Voluntary report
Reporter Location
IN, US
Reporter Occupation
DENTIST

Narratives

Description of Event or Problem · 1

BD SYRINGE USED FOR ORAL LIQUID IN NICU. THE BD AMBER ORAL SYRINGE 1ML IS IN INCREMENTS OF 0.02MG. THERE WAS CONFUSION BECAUSE THE BD IV - CLEAR- LUER LOCK SYRINGE 1ML IS IN INCREMENTS OF 0.01MG. THEREFORE, THE NURSE MISREAD THE ORAL SYRINGE BECAUSE SHE WAS USED TO READING IN 0.01MG INCREMENTS ON THE IV SYRINGE. WOULD SUGGEST INCREMENTS BEING THE SAME -0.01MG- ON BOTH ORAL AND IV 1 ML SYRINGES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BD ORAL AMBER SYRINGE 1 ML NONE KYX

Patients

Seq Age Sex Outcome Treatment
1 15 DA