Fresh Recalls

FDAClass I · Medical device · Recall Z-1947-2026 · Recalled May 6, 2026

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

Agency report date: May 6, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
AIDBAGs are first aid kits of convenience composed of individually labeled devices designe
Company / brand
North American Rescue
Lot / serial / date codes
Kit REF/UDI-DI/Lot: 85-4661/00842209132089/85-4661122024; 85-4742/00842209133536/85-4742123024. Meter: UDI-DI: 20612479197217, all lots.
Distribution
US: CA, WA
Agency product description and boundaries

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).

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: AIDBAGs are first aid kits of convenience composed of individually labeled devices designe recall status

3. Open the official notice or contact

Official recall ID
Z-1947-2026
Brand
All North American Rescue recalls
Classification
Class I
Units affected
21
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Greer, SC, United States
Firm address
35 Tedwall Ct, 29650-4791

Identifying details (verbatim from the notice)

Product codes / lots
Kit REF/UDI-DI/Lot: 85-4661/00842209132089/85-4661122024; 85-4742/00842209133536/85-4742123024. Meter: UDI-DI: 20612479197217, all lots.
Distribution
US: CA, WA
FDA event ID
98697
Recall initiated
March 27, 2026
FDA classified
April 29, 2026
FDA report date
May 6, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 20, 2026 at 6:00 PM UTC. Record retrieved August 4, 2026 at 11:00 PM UTC.

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