FDA Adverse Event Death Summary report: N

HEPARIN LOCK FLUSH SOLUTION 100 UNITS/ML

MDR report key: 1056167 · Received June 3, 2008

Report

Report Number
MW5007122
Event Type
Death
Date Received
June 3, 2008
Date of Event
January 5, 2008
Report Date
June 3, 2008
Manufacturer
AMSINO MEDICAL USA
Product Code
NZW
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

A RESIDENT USED HEPARIN LOCK FLUSH SOLUTION. WE HAVE 2 SYRINGES 100 UNITS -LOT #KH02552 AND #KH02517- THAT NEED TO BE TESTED FOR OCS. COULD YOU PLEASE DIRECT US ON WHERE IT CAN BE TESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEPARIN LOCK FLUSH SOLUTION 100 UNITS/ML NONE NZW AMSINO MEDICAL USA KH02552
2 HEPARIN LOCK FLUSH SOLUTION 100 UNITS/ML NONE NZW AMSINO MEDICAL USA KH02517

Patients

Seq Age Sex Outcome Treatment
1 Death