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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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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 12 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-4756 | FDA UDI | Class I | Active |
| Nar | 80-1483 | FDA UDI | N/A | Active |
| Nar | 80-1129 | FDA UDI | N/A | Active |
| Nar | 85-2432 | FDA UDI | N/A | Active |
| Nar | 80-1437 | FDA UDI | N/A | Active |
| NAR Kit | 85-2919 | FDA UDI | N/A | Active |
| NAR Kit | 70-0195 | FDA UDI | N/A | Active |
| Nar | 85-0488 | FDA UDI | N/A | Active |
| Nar | 80-0524 | FDA UDI | N/A | Active |
| NAR Kit | 85-0415 | FDA UDI | N/A | Active |
| Nar | 85-1528 | FDA UDI | N/A | Active |
| Nar | 85-2812 | FDA UDI | N/A | Active |
| Nar | 85-2573 | FDA UDI | N/A | Active |
| Nar | 85-4268 | FDA UDI | Class I | Active |
| Nar | 80-1135 | FDA UDI | N/A | Active |
| Nar | 85-2720 | FDA UDI | N/A | Active |
| Nar | 85-3393 | FDA UDI | N/A | Active |
| NAR Kit | 80-0424 | FDA UDI | N/A | Active |
| NAR Kit | 85-1636 | FDA UDI | N/A | Active |
| Nar | 85-2057 | FDA UDI | N/A | Active |
| NAR Kit | 85-0052 | FDA UDI | N/A | Active |
| Nar | 85-3830 | FDA UDI | N/A | Active |
| Nar | 10-0037 | FDA UDI | Class I | Active |
| Nar | 85-4260 | FDA UDI | Class I | Active |
| Nar | 80-1023 | FDA UDI | N/A | Active |
| Nar | 85-2212 | FDA UDI | N/A | Active |
| Nar | 80-0494 | FDA UDI | N/A | Active |
| Nar | 80-1738 | FDA UDI | Class I | Active |
| Nar | 85-4241 | FDA UDI | N/A | Active |
| Nar | 85-1616 | FDA UDI | N/A | Active |
| NAR Kit | 85-3232 | FDA UDI | N/A | Active |
| Nar | 85-1784 | FDA UDI | N/A | Active |
| Nar | 80-0868 | FDA UDI | N/A | Active |
| Nar | 85-4902 | FDA UDI | Class I | Active |
| Nar | 85-4845 | FDA UDI | Class I | Active |
| Nar | 77-0094 | FDA UDI | Class I | Active |
| NAR Kit | 85-2240 | FDA UDI | N/A | Active |
| Nar | 85-4159 | FDA UDI | N/A | Active |
| Nar | 85-4066 | FDA UDI | N/A | Active |
| Nar | 85-3964 | FDA UDI | N/A | Active |
| Nar | 85-1964 | FDA UDI | N/A | Active |
| Nar | 80-0460 | FDA UDI | N/A | Active |
| Nar | 85-3527 | FDA UDI | N/A | Active |
| Black Talon | 70-0004 | FDA UDI | Class I | Active |
| Nar | 85-4604 | FDA UDI | N | Active |
| NAR Kit | 80-1202 | FDA UDI | N/A | Active |
| NAR Kit | 85-2324 | FDA UDI | Class II | Active |
| Nar | 85-4431 | FDA UDI | Class I | Active |
| Nar | 85-3370 | FDA UDI | N/A | Active |
| Nar | 85-4704 | 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 |