North American Rescue LLC. recalls AIDBAGs are first aid kits of convenience composed of individually labeled devices designe

Recalling company

North American Rescue LLC.

Product

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 indications, is maintained for each device, which may be used independently and at different times. These specific kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that were recalled as part of RES 98317 with (510(k): K140100).

Reason

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.

Classification

Class I – a reasonable probability that use will cause serious adverse health consequences or death

Recall date

Mar 27, 2026

Reported

May 6, 2026

Distribution

US: CA, WA

Status

Ongoing

Quantity

21

Lot / codes

Kit REF/UDI-DI/Lot: 85-4661/00842209132089/85-4661122024; 85-4742/00842209133536/85-4742123024. Meter: UDI-DI: 20612479197217, all lots.

Company location

Greer, SC

Recall type

Voluntary: Firm initiated

Recall number

Z-1947-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1947-2026 in the FDA Enforcement Report. Also see FDA recall press releases.