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 |