FDA Adverse Event Injury Summary report: N

INRATIO

MDR report key: 1853330 · Received September 30, 2010

Report

Report Number
2027969-2010-01616
Event Type
Injury
Date Received
September 30, 2010
Date of Event
September 14, 2010
Report Date
September 30, 2010
Manufacturer
ALERE SAN DIEGO, INC.
Product Code
GJS
PMA / PMN Number
K021923
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
NOT APPLICABLE

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) 2010, INRATIO: 2.3. METER WAS DROPPED BY CLEANING LADY. DATE: (B)(6) 2010, INRATIO: 4.6. PT SKIPPED TWO COUMADIN DOSES AS INSTRUCTED BY DOCTOR. DATE: (B)(6) 2010, INRATIO: 3.8, RE-TEST: 4.4. RE-TEST WAS DONE ON A DIFFERENT FINGER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INRATIO PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC. 100071 221730

Patients

Seq Age Sex Outcome Treatment
1 Other