Investigation Launched into True Metrix Glucose Monitor Recall: Are You Affected?
Investigation into True Metrix Blood Glucose Monitor Recall
Background on the Recall
On April 28, 2026, the FDA issued a Class I recall for the True Metrix blood glucose monitoring systems produced by Trividia Health, Inc. This recall comes after serious incidents involving at least 114 reported injuries and one fatality. The affected devices include various models: True Metrix, True Metrix Air, True Metrix Go, and True Metrix Pro. These models were flagged for displaying an
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