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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 63 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 80-0282 | FDA UDI | N/A | Unknown |
| Nar | 80-0886 | FDA UDI | N/A | Active |
| NAR Kit | 80-0314 | FDA UDI | N/A | Unknown |
| NAR Kit | 80-0201 | FDA UDI | N/A | Active |
| NAR Kit | 85-1511 | FDA UDI | N/A | Active |
| Nar | 85-2782 | FDA UDI | N/A | Active |
| Nar | 85-2173 | FDA UDI | N/A | Active |
| NAR Kit | 80-0183 | FDA UDI | N/A | Active |
| NAR Kit | 85-3273 | FDA UDI | N/A | Active |
| Nar | 85-3298 | FDA UDI | N/A | Active |
| NAR Kit | 85-2612 | FDA UDI | N/A | Active |
| Nar | 85-3220 | FDA UDI | N/A | Active |
| Nar | 80-1621 | FDA UDI | Class I | Active |
| Nar | 85-3391 | FDA UDI | N/A | Active |
| Nar | 82-0072 | FDA UDI | N | Active |
| Nar | 85-2677 | FDA UDI | N/A | Active |
| Nar | 80-1428 | FDA UDI | Class I | Active |
| Nar | 85-2567 | FDA UDI | N/A | Active |
| NAR Kit | 82-0037 | FDA UDI | N/A | Active |
| Nar | 83-0029 | FDA UDI | Class II | Active |
| Nar | 10-0015 | FDA UDI | Class I | Active |
| Nar | 85-4370 | FDA UDI | Class I | Active |
| Nar | 85-3007 | FDA UDI | N/A | Active |
| NAR Kit | 85-1304 | FDA UDI | N/A | Active |
| Nar | 80-1563 | FDA UDI | N/A | Active |
| Nar | 80-1843 | FDA UDI | Class I | Active |
| Nar | 85-2856 | FDA UDI | N/A | Active |
| Nar | 84-0134 | FDA UDI | N/A | Active |
| Nar | 85-3360 | FDA UDI | N/A | Active |
| Nar | 85-2415 | FDA UDI | N/A | Active |
| Nar | 85-3977 | FDA UDI | N/A | Active |
| NAR Kit | 85-1590 | FDA UDI | N/A | Unknown |
| NAR Kit | 85-3212 | FDA UDI | N/A | Active |
| Nar | 85-2667 | FDA UDI | N/A | Active |
| Nar | 85-4182 | FDA UDI | Class I | Active |
| Nar | 80-1593 | FDA UDI | N | Active |
| Nar | 85-4118 | FDA UDI | N/A | Active |
| Nar | 85-3125 | FDA UDI | N/A | Active |
| Nar | 85-2406 | FDA UDI | N/A | Active |
| Nar | 85-4388 | FDA UDI | N | Active |
| Nar | 85-4189 | FDA UDI | N/A | Active |
| NAR Kit | 85-3296 | FDA UDI | N/A | Active |
| Nar | 80-1564 | FDA UDI | Class I | Active |
| NAR Kit | 80-1188 | FDA UDI | N/A | Active |
| Nar | 85-2872 | FDA UDI | N/A | Active |
| Nar | 80-1500 | FDA UDI | N/A | Active |
| Nar | 85-4296 | FDA UDI | Class I | Active |
| NAR Kit | 85-3327 | FDA UDI | N/A | Active |
| Nar | 80-1708 | FDA UDI | Class I | Active |
| Nar | 85-4664 | 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 |