FDA Adverse Event
Malfunction
Summary report: N
HEPARIN LOCK FLUSH SOLUTION
MDR report key: 1726940
·
Received June 14, 2010
Report
- Report Number
- MW5016380
- Event Type
- Malfunction
- Date Received
- June 14, 2010
- Date of Event
- June 4, 2010
- Report Date
- June 10, 2010
- Manufacturer
- B-D
- Product Code
- NZW
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
I CAME ACROSS A MEDICATION THAT I BELIEVE HAS AN INCORRECT BARCODE. IS THIS THE CORRECT PLACE TO REPORT IT? THE MEDICATION IS: HEPARIN LOCK FLUSH SOLUTION, USP, 10 UNITS/ML. MANUFACTURED BY: BD, (B) (4). (B) (4), (B) (4). THE NDC IS LISTED AS (B) (4). THE BARCODE IS: (B) (4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HEPARIN LOCK FLUSH SOLUTION | HEPARIN LOCK FLUSH SOLUTION, USP, 10 UNITS/ML | NZW | B-D | 007021N |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |