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Sign in to claim this brandNORTH AMERICAN RESCUE, LLC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 35 TEDWALL COURT, Greer, SC, 29650
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 72 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 85-3028 | FDA UDI | N/A | Active |
| NAR Kit | 85-2809 | FDA UDI | N/A | Active |
| NAR Kit | 80-0299 | FDA UDI | N/A | Active |
| NAR Kit | 85-0653 | FDA UDI | N/A | Active |
| NAR Kit | 80-0564 | FDA UDI | N/A | Active |
| NAR Kit | 80-1179 | FDA UDI | N/A | Active |
| NAR Kit | 80-0503 | FDA UDI | N/A | Active |
| NAR Kit | 85-0935 | FDA UDI | N/A | Active |
| NAR Kit | ZZ-1360 | FDA UDI | Class I | Active |
| NAR Kit | 80-1074 | FDA UDI | N/A | Active |
| NAR Kit | 85-1419 | FDA UDI | N/A | Active |
| NAR Kit | 85-2801 | FDA UDI | N/A | Active |
| NAR Kit | 85-0564 | FDA UDI | N/A | Active |
| NAR Kit | 85-0766 | FDA UDI | N/A | Active |
| NAR Kit | 80-1037 | FDA UDI | N/A | Active |
| NAR Kit | 80-0251 | FDA UDI | N/A | Active |
| NAR Kit | 85-2636 | FDA UDI | N/A | Active |
| NAR Kit | 82-0053 | FDA UDI | N/A | Active |
| NAR Kit | 85-2201 | FDA UDI | N/A | Active |
| NAR Kit | 82-0038 | FDA UDI | N/A | Active |
| NAR Kit | 85-0410 | FDA UDI | N/A | Active |
| NAR Kit | 85-2643 | FDA UDI | N/A | Active |
| NAR Kit | 85-1942 | FDA UDI | N/A | Active |
| NAR Kit | 85-2826 | FDA UDI | N/A | Active |
| NAR Kit | 85-3540 | FDA UDI | N/A | Active |
| NAR Kit | 80-0523 | FDA UDI | N/A | Active |
| NAR Kit | 85-1308 | FDA UDI | N/A | Active |
| NAR Kit | 85-1588 | FDA UDI | N/A | Active |
| NAR Kit | 85-3606 | FDA UDI | N/A | Active |
| NAR Kit | 85-1592 | FDA UDI | N/A | Active |
| NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six | K152340 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (4)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 27, 2026 | Z-1947-2026 | — | open, 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. |
| Jul 1, 2025 | Z-2637-2025 | — | open, classified | Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use. |
| Aug 27, 2021 | Z-2520-2021 | — | terminated | The device includes the incorrect Instructions for Use. |
| Aug 21, 2020 | Z-3018-2020 | — | terminated | Lack of sterility assurance of the 30-0171 |