Alere INRatio News - Product Recall
Alere INRatio News
  • FDA Recalls Alere INRatio and INRatio2 Monitor Systems

    Yet another recall has been made on the heels of serious and traumatic device malfunctions- nearly 19,000 reports, to be exact. The recall for Alere INRatio and INRatio2 by the Food and Drug Administration has been upgraded to a Class I recall, meaning use of the product could cause serious or adverse health consequences and even death.

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