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 |