FDA Adverse Event Malfunction Summary report: N

INRATIO

MDR report key: 2010228 · Received February 11, 2011

Report

Report Number
2027969-2011-00301
Event Type
Malfunction
Date Received
February 11, 2011
Date of Event
January 17, 2011
Report Date
February 10, 2011
Manufacturer
ALERE SAN DIEGO, INC
Product Code
GJS
PMA / PMN Number
021923
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION PENDING.

Description of Event or Problem · 1

CALLER ALLEGED DISCREPANT RESULTS COMPARED WITH THE LAB. RESULTS AS FOLLOWS: DATE: (B)(6) 2011, INRATIO: 1.0, LAB: 2.3.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INRATIO PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC 100139 237432

Patients

Seq Age Sex Outcome Treatment
1 NI