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