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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 3 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 85-2932 | FDA UDI | N/A | Active |
| Nar | 85-4910 | FDA UDI | Class I | Active |
| Nar | 85-1982 | FDA UDI | N/A | Active |
| Nar | 85-4785 | FDA UDI | Class I | Active |
| Nar | 85-4153 | FDA UDI | N/A | Active |
| Nar | 85-4461 | FDA UDI | Class I | Active |
| NAR Kit | 85-3035 | FDA UDI | N/A | Active |
| NAR Kit | 85-1913 | FDA UDI | N/A | Active |
| Nar | 85-4881 | FDA UDI | Class I | Active |
| NAR Kit | 85-3112 | FDA UDI | N/A | Active |
| Nar | 85-3593 | FDA UDI | N/A | Active |
| Nar | 85-2906 | FDA UDI | N/A | Active |
| Nar | 85-3502 | FDA UDI | N/A | Active |
| Nar | 85-4244 | FDA UDI | N/A | Active |
| Nar | 80-1814 | FDA UDI | Class I | Active |
| Nar | 85-4723 | FDA UDI | N | Active |
| Nar | 82-0069 | FDA UDI | N | Active |
| Nar | 80-1617 | FDA UDI | Class I | Active |
| Nar | 80-1107 | FDA UDI | N/A | Active |
| Nar | 85-2857 | FDA UDI | N/A | Active |
| NAR Kit | 80-1152 | FDA UDI | N/A | Active |
| Nar | 85-3340 | FDA UDI | N/A | Active |
| Nar | 80-0993 | FDA UDI | N/A | Active |
| NAR Kit | 85-2845 | FDA UDI | N/A | Active |
| NAR Kit | 85-1959 | FDA UDI | N/A | Active |
| Nar | 80-1217 | FDA UDI | Class I | Active |
| Nar | 85-2961 | FDA UDI | N/A | Active |
| NAR Kit | 80-1166 | FDA UDI | N/A | Active |
| Nar | 85-2069-TLS | FDA UDI | Class I | Active |
| Nar | 85-3139 | FDA UDI | N/A | Active |
| Nar | 80-0991 | FDA UDI | N/A | Active |
| Nar | 85-2766 | FDA UDI | N/A | Active |
| Nar | 10-0073 | FDA UDI | Class I | Active |
| Nar | 85-3386 | FDA UDI | N/A | Active |
| NAR Kit | 85-1971 | FDA UDI | N/A | Active |
| NAR kit | 84-0092 | FDA UDI | N/A | Active |
| Nar | 85-3428 | FDA UDI | Class I | Active |
| NAR Kit | 85-2641 | FDA UDI | N/A | Active |
| Nar | 30-0052 | FDA UDI | Class I | Active |
| Nar | 35-0025 | FDA UDI | Class I | Active |
| Nar | 85-3461 | FDA UDI | N/A | Active |
| Nar | 85-4925 | FDA UDI | Class I | Active |
| NAR Kit | 80-0071 | FDA UDI | N/A | Active |
| Nar | 85-3483 | FDA UDI | N/A | Active |
| Nar | 82-0073 | FDA UDI | N | Active |
| Nar | 20-0018 | FDA UDI | Class I | Active |
| Nar | 85-4261 | FDA UDI | N/A | Active |
| Nar | 85-2076 | FDA UDI | N/A | Active |
| Nar | 85-4713 | FDA UDI | Class I | Active |
| NAR Kit | 85-1593 | FDA UDI | N/A | Active |
Related Companies
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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 |