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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 29 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-3958 | FDA UDI | N/A | Active |
| Nar | 85-3178 | FDA UDI | N/A | Active |
| NAR Kit | 80-0283 | FDA UDI | N/A | Active |
| NAR Kit | 85-2234 | FDA UDI | N/A | Active |
| Nar | 85-4042 | FDA UDI | N/A | Active |
| Nar | 85-4152 | FDA UDI | N/A | Active |
| NAR Kit | 85-2419 | FDA UDI | N/A | Active |
| Nar | 85-4663 | FDA UDI | Class I | Active |
| Nar | 85-4668 | FDA UDI | Class I | Active |
| Nar | 85-1470 | FDA UDI | N/A | Active |
| Nar | ZZ-1674 | FDA UDI | Class I | Active |
| NAR Kit | 85-1679 | FDA UDI | N/A | Active |
| Nar | 85-3572 | FDA UDI | N/A | Active |
| Nar | 85-3885 | FDA UDI | N/A | Active |
| NAR Kit | 80-0976 | FDA UDI | N/A | Active |
| Nar | 80-1595 | FDA UDI | Class I | Active |
| Nar | 85-3945 | FDA UDI | N/A | Active |
| NAR Kit | 80-1147 | FDA UDI | N/A | Active |
| Nar | 85-3348 | FDA UDI | N/A | Active |
| Nar | 85-3986 | FDA UDI | N/A | Active |
| Nar | 85-3895 | FDA UDI | N/A | Active |
| Nar | 80-1453 | FDA UDI | Class I | Active |
| Nar | 85-4025 | FDA UDI | N/A | Active |
| Nar | 85-1697 | FDA UDI | N/A | Active |
| NAR Kit | 85-1479 | FDA UDI | N/A | Active |
| Nar | 85-2412 | FDA UDI | N/A | Active |
| Nar | 85-3396 | FDA UDI | N/A | Active |
| Nar | 85-3197 | FDA UDI | N/A | Active |
| NAR Kit | 85-3783 | FDA UDI | N/A | Active |
| Nar | 88-0029 | FDA UDI | Class I | Active |
| Nar | 85-4714 | FDA UDI | Class I | Active |
| Nar | 85-4090 | FDA UDI | N/A | Active |
| Nar | 85-4207 | FDA UDI | Class I | Active |
| NAR Kit | 82-0031 | FDA UDI | N/A | Active |
| Nar | 88-0037 | FDA UDI | Class I | Active |
| NAR Kit | 85-0538 | FDA UDI | N/A | Active |
| Nar | 85-4412 | FDA UDI | Class I | Active |
| NAR Kit | 85-2079 | FDA UDI | N/A | Active |
| Nar | 85-1812 | FDA UDI | N/A | Active |
| NAR Kit | 85-1356 | FDA UDI | N/A | Active |
| NAR Kit | 85-2603 | FDA UDI | N/A | Active |
| NAR Kit | 80-1200 | FDA UDI | N/A | Active |
| NAR Kit | 85-1900 | FDA UDI | N/A | Active |
| Nar | 85-3643 | FDA UDI | N/A | Active |
| Nar | 85-4504 | FDA UDI | Class I | Active |
| Nar | 85-3795 | FDA UDI | N/A | Active |
| Nar | 85-2913 | FDA UDI | N/A | Active |
| Nar | 85-3402 | FDA UDI | N/A | Active |
| Nar | 80-1673 | FDA UDI | Class I | Active |
| Nar | 85-4522 | FDA UDI | Class I | 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 |