FDA Adverse Event Malfunction Summary report: N

INRATIO

MDR report key: 1935163 · Received December 6, 2010

Report

Report Number
2027969-2010-02116
Event Type
Malfunction
Date Received
December 6, 2010
Date of Event
October 8, 2010
Report Date
December 6, 2010
Manufacturer
ALERE SAN DIEGO, INC
Product Code
GJS
PMA / PMN Number
021923
Removal / Correction Number
NI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION PENDING.

Description of Event or Problem · 1

CALLER ALLEGED IMPRECISION WITH INRATIO METER. RESULTS AS FOLLOWS: DATE: (B)(6) 2010, INR: 1.7. DATE: (B)(6) 2010, INR: 2.9. PT WAS STABLE FOR 3 MONTHS ON THE INRATIO METER UNTIL RESULTS ON (B)(6) 2010.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 NI