FDAJuly 11, 2016device

Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A Product Usage: The Alere INRatio¿/INRatio¿2 system uses a modified version of the one-stage PT test. After a drop of blood is applied to the test strip, it is drawn into the test area and mixed with reagents that initiate c...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Alere San Diego is initiating a voluntary recall for the Alere INRatio¿/INRatio¿2 PT/INR Monitoring Systems (Test Strips and Meters). This action is being initiated as a result of patients who had a therapeutic or near-therapeutic INR with the Alere INRatio¿/INRatio¿2 PT/INR Monitoring System but a significantly higher INR (outside of therapeutic range) when performed by a central laboratory.

What to do

FDA enforcement status: Terminated

Brands named

alere san diegoalerealere san

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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