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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 36 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-2168 | FDA UDI | N/A | Active |
| Nar | 85-1417 | FDA UDI | N/A | Active |
| Nar | 85-1657 | FDA UDI | N/A | Active |
| Nar | 85-2726 | FDA UDI | N/A | Active |
| NAR Kit | 10-0052 | FDA UDI | Class II | Active |
| Nar | 85-2331 | FDA UDI | N/A | Active |
| Nar | 80-1694 | FDA UDI | Class I | Active |
| Nar | 85-4879 | FDA UDI | Class I | Active |
| Nar | 85-3395 | FDA UDI | N/A | Active |
| NAR Kit | 85-3013 | FDA UDI | N/A | Active |
| Nar | 80-0474 | FDA UDI | N/A | Active |
| Nar | 20-0100 | FDA UDI | Class I | Active |
| Nar | 80-1101 | FDA UDI | N/A | Active |
| Nar | 80-0027 | FDA UDI | Class I | Active |
| Nar | 80-0881 | FDA UDI | N/A | Active |
| Nar | 85-4477 | FDA UDI | N | Active |
| NAR Kit | 80-0293 | FDA UDI | N/A | Unknown |
| Nar | 85-3845 | FDA UDI | N/A | Active |
| NAR Kit | 80-0889 | FDA UDI | N/A | Active |
| NAR Kit | 80-1069 | FDA UDI | N/A | Active |
| Nar | 80-0471 | FDA UDI | N/A | Active |
| Nar | 85-4149 | FDA UDI | N/A | Active |
| NAR Kit | 85-3019 | FDA UDI | N/A | Active |
| Nar | 80-1836 | FDA UDI | N | Active |
| Nar | 84-0136 | FDA UDI | N/A | Active |
| NAR Kit | 85-2302 | FDA UDI | N/A | Active |
| Nar | 85-3675 | FDA UDI | N/A | Active |
| Nar | 80-1127 | FDA UDI | N/A | Active |
| NAR Kit | 85-3067 | FDA UDI | N/A | Active |
| Nar | 85-4119 | FDA UDI | Class I | Active |
| Nar | 80-1648 | FDA UDI | Class I | Active |
| Nar | 85-3555 | FDA UDI | N/A | Active |
| Nar | 80-1214 | FDA UDI | N/A | Active |
| Nar | 80-1802 | FDA UDI | Class I | Active |
| Nar | 85-2577 | FDA UDI | N/A | Active |
| Nar | 85-4361 | FDA UDI | Class I | Active |
| Nar | 85-4298 | FDA UDI | Class I | Active |
| NAR Kit | 85-1969 | FDA UDI | N/A | Active |
| NAR Kit | 85-3420 | FDA UDI | N/A | Active |
| Nar | 80-1575 | FDA UDI | N/A | Active |
| Nar | 85-4283 | FDA UDI | Class I | Active |
| Nar | 85-3658 | FDA UDI | N/A | Active |
| Nar | 85-3338 | FDA UDI | N/A | Active |
| NAR Kit | 85-2252 | FDA UDI | N/A | Active |
| Nar | 20-0012 | FDA UDI | Class I | Active |
| NAR Kit | 85-2495 | FDA UDI | N/A | Active |
| Nar | 85-4116 | FDA UDI | N/A | Active |
| Nar | 30-0171 | FDA UDI | Class I | Active |
| NAR Kit | 85-0182 | FDA UDI | N/A | Unknown |
| Nar | 85-3388 | 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 |