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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 25 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 85-1791 | FDA UDI | N/A | Active |
| Nar | 85-4478 | FDA UDI | Class I | Active |
| Nar | 87-0001 | FDA UDI | Class I | Active |
| Nar | 80-1024 | FDA UDI | N/A | Active |
| NAR Kit | 80-1154 | FDA UDI | N/A | Active |
| Nar | 85-4803 | FDA UDI | Class I | Active |
| Nar | 85-4460 | FDA UDI | Class I | Active |
| Nar | 85-4002 | FDA UDI | Class I | Active |
| Nar | 85-4635 | FDA UDI | Class I | Active |
| Nar | 85-4822 | FDA UDI | Class I | Active |
| Nar | 85-3998 | FDA UDI | N/A | Active |
| Nar | 85-4161 | FDA UDI | N/A | Active |
| Nar | 80-1496 | FDA UDI | N/A | Active |
| Nar | 80-1157 | FDA UDI | N/A | Active |
| Nar | 80-1684 | FDA UDI | Class I | Active |
| Nar | 84-0175 | FDA UDI | Class I | Active |
| Nar | 80-1569 | FDA UDI | N/A | Active |
| Nar | 85-4331 | FDA UDI | Class I | Active |
| Nar | 30-0292 | FDA UDI | Class I | Active |
| Nar | 85-4367 | FDA UDI | Class I | Active |
| NAR Kit | 80-0916 | FDA UDI | N/A | Unknown |
| Nar | 85-3850 | FDA UDI | N/A | Active |
| Nar | 85-1515 | FDA UDI | N/A | Active |
| Nar | 85-3000 | FDA UDI | N/A | Active |
| NAR Kit | 85-3199 | FDA UDI | N/A | Active |
| Nar | 30-0165 | FDA UDI | Class I | Active |
| Nar | 80-1676 | FDA UDI | Class I | Active |
| Nar | 85-4601 | FDA UDI | Class I | Active |
| Nar | 85-4399 | FDA UDI | Class I | Active |
| NAR Kit | 30-0046 | FDA UDI | Class II | Active |
| NAR Kit | 80-1233 | FDA UDI | N/A | Active |
| NAR Kit | 85-0693 | FDA UDI | N/A | Active |
| Nar | 85-1646 | FDA UDI | N/A | Active |
| NAR Kit | 85-1709 | FDA UDI | N/A | Active |
| NAR Kit | 85-3287 | FDA UDI | N/A | Active |
| NAR Kit | 85-2661 | FDA UDI | N/A | Active |
| Nar | 85-3963 | FDA UDI | N/A | Active |
| Nar | 85-4971 | FDA UDI | Class I | Active |
| Nar | 85-0716 | FDA UDI | N/A | Active |
| Nar | 85-4743 | FDA UDI | Class I | Active |
| Nar | 85-3856 | FDA UDI | N/A | Active |
| Nar | 85-2465 | FDA UDI | N/A | Active |
| Nar | 85-3329 | FDA UDI | N/A | Active |
| Nar | 85-3635 | FDA UDI | N/A | Active |
| Nar | 85-3324 | FDA UDI | N/A | Active |
| NAR Kit | 85-3016 | FDA UDI | N/A | Active |
| Nar | 85-2074 | FDA UDI | N/A | Active |
| Nar | 82-0070 | FDA UDI | N | Active |
| Nar | 85-4828 | FDA UDI | Class I | Active |
| NAR Kit | 85-3268 | 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 |