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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 10 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-4871 | FDA UDI | Class I | Active |
| Nar | 85-3389 | FDA UDI | N/A | Active |
| Nar | 85-2476 | FDA UDI | N/A | Active |
| Nar | 85-4095 | FDA UDI | N/A | Active |
| Nar | 80-1614 | FDA UDI | N | Active |
| NAR Kit | 85-1981 | FDA UDI | N/A | Active |
| Nar | 85-2374 | FDA UDI | N/A | Active |
| Nar | 85-3191 | FDA UDI | N/A | Active |
| NAR Kit | 85-2180 | FDA UDI | N/A | Active |
| Nar | 85-1800 | FDA UDI | N/A | Active |
| Nar | 80-1719 | FDA UDI | Class I | Active |
| NAR Kit | 80-0439 | FDA UDI | N/A | Active |
| NAR Kit | 85-2249 | FDA UDI | N/A | Active |
| Nar | 85-1567 | FDA UDI | N/A | Active |
| Nar | 80-1750 | FDA UDI | Class I | Active |
| Nar | 85-4563 | FDA UDI | Class I | Active |
| NAR Kit | 85-1671 | FDA UDI | N/A | Active |
| Nar | 80-0578 | FDA UDI | N/A | Active |
| Nar | 85-2954 | FDA UDI | N/A | Active |
| Nar | 85-3062 | FDA UDI | N/A | Active |
| Nar | 85-2948 | FDA UDI | N/A | Active |
| Nar | 77-0078 | FDA UDI | Class I | Active |
| Nar | 85-4899 | FDA UDI | Class I | Active |
| Nar | 85-3813 | FDA UDI | N/A | Active |
| Nar | 10-0042 | FDA UDI | Class I | Active |
| NAR Kit | 85-1907 | FDA UDI | N/A | Active |
| Nar | 85-4659 | FDA UDI | Class I | Active |
| NAR Kit | 80-0003 | FDA UDI | N/A | Active |
| NAR Kit | 85-3566 | FDA UDI | N/A | Active |
| Nar | 85-3629 | FDA UDI | N/A | Active |
| NAR Kit | 85-2548 | FDA UDI | N/A | Active |
| Nar | 85-2958 | FDA UDI | N/A | Active |
| Nar | 30-0094 | FDA UDI | Class I | Active |
| Nar | 85-3975 | FDA UDI | N/A | Active |
| NAR Kit | 85-3102 | FDA UDI | N/A | Active |
| Nar | 85-2401 | FDA UDI | N/A | Active |
| NAR Kit | 85-1458 | FDA UDI | N/A | Active |
| Nar | 85-3859 | FDA UDI | N/A | Active |
| Nar | 85-4353 | FDA UDI | Class I | Active |
| Nar | 85-4172 | FDA UDI | N/A | Active |
| Nar | 85-3222 | FDA UDI | N/A | Active |
| Nar | 85-2054 | FDA UDI | N/A | Active |
| Nar | 85-3336 | FDA UDI | N/A | Active |
| Nar | 80-0891 | FDA UDI | N/A | Active |
| Nar | 80-0496 | FDA UDI | N/A | Active |
| Nar | 80-1124 | FDA UDI | N/A | Active |
| Nar | 80-1818 | FDA UDI | Class I | Active |
| Nar | 85-3969 | FDA UDI | N/A | Active |
| NAR Kit | 85-2296 | FDA UDI | N/A | Active |
| Nar | 80-1706 | FDA UDI | Class I | 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 |