FDAMarch 27, 2026device

AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the appropriate level provider to evaluate and treat patients at the point-of-injury / point-of-illness. The original manufacturer labeling, including single use in...

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

The hazard

Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the meter displays an E-5 error code for a very high blood glucose event (> 600 mg/dL) or when there is a test strip error, which can lead to operator confusion when evaluating patients and a delay in appropriate treatment. This is a downstream recall of Trividia Health Class I, Recall Event ID 98317.

What to do

FDA enforcement status: Ongoing

Brands named

north american rescuenorthnorth american

UPCs

008422091320898546611220240084220913353685474212302420612479197217

Recall history

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

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