FDA Adverse Event Malfunction Summary report: N

INRATIO

MDR report key: 2231279 · Received July 25, 2011

Report

Report Number
2027969-2011-01627
Event Type
Malfunction
Date Received
July 25, 2011
Date of Event
June 21, 2011
Report Date
July 25, 2011
Manufacturer
ALERE SAN DIEGO, INC
Product Code
GJS
PMA / PMN Number
K021923
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

PENDING.

Description of Event or Problem · 1

CUSTOMER ALLEGES DISCREPANT RESULTS WITH METER: SEE SCANNED TABLE. PT'S TARGET RANGE IS 2.5 - 3.5. COMPARISONS DONE WITHIN MINUTES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INRATIO PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC 100071 243104

Patients

Seq Age Sex Outcome Treatment
1