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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 43 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-4652 | FDA UDI | Class I | Active |
| Nar | 85-2945 | FDA UDI | N/A | Active |
| Nar | 80-1451 | FDA UDI | Class I | Active |
| NAR Kit | 80-1059 | FDA UDI | N/A | Active |
| Nar | 85-1945 | FDA UDI | N/A | Active |
| Nar | 85-2435 | FDA UDI | N/A | Active |
| NAR Kit | 85-1884 | FDA UDI | N/A | Active |
| NAR Kit | 85-2565 | FDA UDI | N/A | Active |
| Nar | 85-3462 | FDA UDI | N/A | Active |
| Nar | 85-3485 | FDA UDI | N/A | Active |
| NAR Kit | 82-0056 | FDA UDI | N/A | Active |
| Nar | 85-4706 | FDA UDI | Class I | Active |
| Nar | 85-4880 | FDA UDI | Class I | Active |
| Nar | 85-3913 | FDA UDI | N/A | Active |
| NAR Kit | 85-3069 | FDA UDI | N/A | Active |
| Nar | 85-4450 | FDA UDI | Class I | Active |
| Nar | 85-4496 | FDA UDI | Class I | Active |
| NAR Kit | 85-2689 | FDA UDI | N/A | Active |
| NAR Kit | 85-0368 | FDA UDI | N/A | Active |
| NAR Kit | 85-0104 | FDA UDI | N/A | Active |
| NAR Kit | 80-0915 | FDA UDI | N/A | Unknown |
| NAR Kit | 80-0454 | FDA UDI | N/A | Active |
| Nar | 85-4937 | FDA UDI | Class I | Active |
| Nar | 85-4459 | FDA UDI | Class I | Active |
| Nar | 85-4318 | FDA UDI | Class I | Active |
| Nar | 85-2273 | FDA UDI | N/A | Active |
| Nar | 80-1136 | FDA UDI | N/A | Active |
| Nar | 85-4800 | FDA UDI | Class I | Active |
| NAR Kit | 80-0440 | FDA UDI | N/A | Active |
| Nar | 80-1808 | FDA UDI | N | Active |
| Nar | 80-0856 | FDA UDI | N/A | Active |
| Nar | 85-3507 | FDA UDI | N/A | Active |
| Nar | 85-1514 | FDA UDI | N/A | Active |
| NAR Kit | 80-0204 | FDA UDI | N/A | Active |
| NAR Kit | 85-1299 | FDA UDI | N/A | Active |
| Nar | 80-1681 | FDA UDI | Class I | Active |
| Nar | 85-2879 | FDA UDI | N/A | Active |
| Nar | 84-0138 | FDA UDI | N/A | Active |
| NAR Kit | 85-2937 | FDA UDI | N/A | Active |
| NAR Kit | 85-1498 | FDA UDI | N/A | Active |
| Nar | 80-1833 | FDA UDI | N | Active |
| Nar | 85-3989 | FDA UDI | N/A | Active |
| NAR Kit | 80-1029 | FDA UDI | N/A | Active |
| Nar | 85-2935 | FDA UDI | N/A | Active |
| Nar | 82-0080 | FDA UDI | N | Active |
| Nar | 85-2960 | FDA UDI | N/A | Active |
| Nar | 85-1723 | FDA UDI | N/A | Active |
| Nar | 80-1838 | FDA UDI | N | Active |
| Nar | 84-0137 | FDA UDI | N/A | Active |
| Nar | 85-4124 | FDA UDI | N/A | 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 |