NARRecalls & reported problems across all models

We found 2 models of NAR by North American Rescue, LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

NAR recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Mar 27, 2026Open, Classified

   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.

   Z-1947-2026 · Root cause: Component design/selection · names 2 of these models · Recall details · FDA record ↗

NAR models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• NAR 85-4661

  First Aid Kit With Drug
  1 recall0 reports
• NAR 85-4742

  First Aid Kit With Drug
  1 recall0 reports

Other North American Rescue, LLC products

• NAR Kit5 models · 0 reports · 1 recall