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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 31 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 85-0190 | FDA UDI | N/A | Active |
| NAR Kit | 85-2489 | FDA UDI | N/A | Active |
| Nar | 85-4908 | FDA UDI | Class I | Active |
| NAR Kit | 85-1757 | FDA UDI | N/A | Active |
| NAR Kit | 85-3205 | FDA UDI | N/A | Active |
| NAR Kit | 85-2544 | FDA UDI | N/A | Active |
| Nar | 85-4386 | FDA UDI | Class I | Active |
| Nar | 85-4697 | FDA UDI | Class I | Active |
| Nar | 80-0951 | FDA UDI | N/A | Active |
| Nar | 85-4580 | FDA UDI | Class I | Active |
| Nar | 85-2259 | FDA UDI | N/A | Active |
| Nar | 85-3631 | FDA UDI | N/A | Active |
| Nar | 84-0127 | FDA UDI | N/A | Active |
| NAR Kit | 85-3367 | FDA UDI | N/A | Active |
| Nar | 85-3413 | FDA UDI | N/A | Active |
| Nar | 85-4877 | FDA UDI | Class I | Active |
| NAR Kit | 85-3377 | FDA UDI | N/A | Active |
| Nar | 85-4282 | FDA UDI | Class I | Active |
| Nar | 85-2198 | FDA UDI | N/A | Active |
| Nar | 85-3337 | FDA UDI | N/A | Active |
| Nar | 85-4427 | FDA UDI | Class I | Active |
| Nar | 85-4726 | FDA UDI | Class I | Active |
| Nar | 80-1652 | FDA UDI | Class I | Active |
| Nar | 85-4048 | FDA UDI | N/A | Active |
| Nar | 85-1887 | FDA UDI | N/A | Active |
| NAR Kit | 85-1315 | FDA UDI | N/A | Active |
| Nar | 80-0510 | FDA UDI | N/A | Active |
| NAR Kit | 80-1075 | FDA UDI | N/A | Active |
| Nar | 85-2884 | FDA UDI | N/A | Active |
| Nar | 80-1702 | FDA UDI | Class I | Active |
| NAR Kit | 85-2540 | FDA UDI | N/A | Active |
| NAR Kit | 85-1379 | FDA UDI | N/A | Unknown |
| NAR Kit | 85-1625 | FDA UDI | N/A | Active |
| Nar | 85-2702 | FDA UDI | N/A | Active |
| Nar | 85-4114 | FDA UDI | N/A | Active |
| NAR Kit | 85-3474 | FDA UDI | N/A | Active |
| Nar | 85-0717 | FDA UDI | N/A | Active |
| Nar | 85-2882 | FDA UDI | N/A | Active |
| NAR Kit | 85-3417 | FDA UDI | N/A | Active |
| Nar | 85-4365 | FDA UDI | Class I | Active |
| Nar | 85-0982 | FDA UDI | N/A | Active |
| Nar | 85-4615 | FDA UDI | Class I | Active |
| Nar | 85-4139 | FDA UDI | N/A | Active |
| Nar | 80-1650 | FDA UDI | N | Active |
| Nar | 80-1427 | FDA UDI | Class I | Active |
| Nar | 85-4934 | FDA UDI | Class I | Active |
| NAR Kit | 85-2496 | FDA UDI | N/A | Active |
| Nar | 85-4252 | FDA UDI | Class I | Active |
| Nar | 85-3931 | FDA UDI | N/A | Active |
| Nar | 85-4669 | FDA UDI | N | Active |
Related Companies
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Importers
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Notified Bodies
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Authorities
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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 |