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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 14 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 77-0107 | FDA UDI | Class I | Active |
| Nar | 85-4125 | FDA UDI | N/A | Active |
| Nar | 85-3934 | FDA UDI | N/A | Active |
| NAR Kit | 85-1930 | FDA UDI | N/A | Active |
| NAR Kit | 85-3642 | FDA UDI | N/A | Active |
| Nar | 80-1103 | FDA UDI | N/A | Active |
| NAR Kit | 85-1484 | FDA UDI | N/A | Active |
| Nar | 83-0035 | FDA UDI | Class II | Active |
| Nar | 85-4346 | FDA UDI | Class I | Active |
| Nar | 85-1466 | FDA UDI | N/A | Active |
| NAR Kit | 85-0139 | FDA UDI | N/A | Active |
| Nar | 85-1529 | FDA UDI | N/A | Active |
| Nar | 85-2787 | FDA UDI | N/A | Active |
| Nar | 85-3546 | FDA UDI | N/A | Active |
| Nar | 85-4070 | FDA UDI | N/A | Active |
| NAR Kit | 85-3278 | FDA UDI | N/A | Active |
| NAR Kit | 85-0050 | FDA UDI | N/A | Active |
| TACTICAL CricKIT | 10-0017 | FDA UDI | Class II | Active |
| NAR Kit | 85-2870 | FDA UDI | N/A | Active |
| NAR Kit | 85-2765 | FDA UDI | N/A | Active |
| NAR Kit | 80-0366 | FDA UDI | N/A | Unknown |
| Nar | 85-2521 | FDA UDI | N/A | Active |
| Nar | 80-0465-TLS | FDA UDI | Class I | Active |
| Nar | 85-3133 | FDA UDI | N/A | Active |
| Nar | 85-4827 | FDA UDI | Class I | Active |
| Nar | 85-0543 | FDA UDI | N/A | Active |
| Nar | 80-1685 | FDA UDI | Class I | Active |
| Nar | 85-4885 | FDA UDI | Class I | Active |
| Nar | 80-1754 | FDA UDI | Class I | Active |
| Nar | 85-1972 | FDA UDI | Class I | Active |
| Nar | 85-4321 | FDA UDI | Class I | Active |
| Nar | 85-3881 | FDA UDI | N/A | Active |
| Nar | 85-1500 | FDA UDI | N/A | Active |
| NAR Kit | 85-2592 | FDA UDI | N/A | Active |
| Nar | 85-3696 | FDA UDI | N/A | Active |
| Nar | 85-4875 | FDA UDI | Class I | Active |
| Nar | 85-4755 | FDA UDI | Class I | Active |
| Nar | 85-2036 | FDA UDI | N/A | Active |
| NAR Kit | 85-3565 | FDA UDI | N/A | Active |
| Nar | 85-1400 | FDA UDI | Class I | Active |
| Nar | 85-4343 | FDA UDI | Class I | Active |
| Nar | 85-4104 | FDA UDI | N/A | Active |
| Nar | 85-4358 | FDA UDI | Class I | Active |
| Nar | 85-3357 | FDA UDI | N/A | Active |
| Nar | 82-0068 | FDA UDI | N | Active |
| Nar | 85-3297 | FDA UDI | N/A | Active |
| Nar | 30-0032 | FDA UDI | Class I | Active |
| Nar | 85-3475 | FDA UDI | N/A | Active |
| Nar | 80-0971 | FDA UDI | N/A | Active |
| Nar | 85-3639 | 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 |