FDA Adverse Event Malfunction Summary report: N

INRATIO2

MDR report key: 1945861 · Received December 27, 2010

Report

Report Number
2027969-2010-02282
Event Type
Malfunction
Date Received
December 27, 2010
Date of Event
December 7, 2010
Report Date
December 27, 2010
Manufacturer
ALERE SAN DIEGO, INC.
Product Code
GJS
PMA / PMN Number
K072727
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION PENDING.

Description of Event or Problem · 1

CUSTOMER ALLEGES DISCREPANT RESULTS WITH METER COMPARED TO LAB: DATE: (B)(6) 2010, INRATIO: 1.0, LAB: 2.39. PT'S TARGET THERAPEUTIC RANGE IS 2.0-3.0. PT'S HEMATOCRIT= 46.4%.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INRATIO2 PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC. 100139 NG

Patients

Seq Age Sex Outcome Treatment
1