Official recall record

AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the app

US FDA — Medical Devices · 2026-03-27 · United StatesClass I

Issuing authority: US FDA — Medical Devices
Alert date: 2026-03-27
Country of alert: United States
Alert level: Class I
Alert type: recall
Barcode (EAN/GTIN): 00842209132089
Brand on record: North American Rescue LLC.

What the authority reported

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

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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