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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 51 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-4075 | FDA UDI | N/A | Active |
| Nar | 85-3723 | FDA UDI | N/A | Active |
| NAR Kit | 80-0987 | FDA UDI | N/A | Active |
| Nar | 85-4077 | FDA UDI | Class I | Active |
| Nar | 85-4533 | FDA UDI | N | Active |
| Nar | 85-3863 | FDA UDI | N/A | Active |
| NAR Kit | 85-1805 | FDA UDI | N/A | Active |
| NAR Kit | 85-1954 | FDA UDI | N/A | Active |
| Nar | 85-2881 | FDA UDI | N/A | Active |
| NAR Kit | 80-0289 | FDA UDI | N/A | Active |
| Nar | 85-4904 | FDA UDI | N | Active |
| NAR Kit | 85-1645 | FDA UDI | N/A | Unknown |
| Nar | 80-1765 | FDA UDI | Class I | Active |
| Nar | 85-4521 | FDA UDI | Class I | Active |
| NAR Kit | 85-3245 | FDA UDI | N/A | Active |
| Nar | 85-2621 | FDA UDI | N/A | Active |
| Nar | ZZ-0042 | FDA UDI | Class I | Active |
| Nar | 85-3883 | FDA UDI | N/A | Active |
| NAR Kit | 83-0020 | FDA UDI | N/A | Active |
| Nar | 85-2770 | FDA UDI | N/A | Active |
| Nar | 85-2947 | FDA UDI | N/A | Active |
| NAR Kit | 80-1078 | FDA UDI | N/A | Active |
| NAR Kit | 85-2112 | FDA UDI | N/A | Active |
| Nar | 85-3290 | FDA UDI | N/A | Active |
| Nar | 80-1852 | FDA UDI | Class II | Active |
| Nar | 85-1202 | FDA UDI | N/A | Active |
| Nar | 84-0153 | FDA UDI | Class I | Active |
| Nar | 80-1703 | FDA UDI | Class I | Active |
| Nar | 85-2751 | FDA UDI | N/A | Active |
| NAR Kit | 82-0002 | FDA UDI | N/A | Active |
| Nar | 80-1826 | FDA UDI | N | Active |
| Nar | 85-4689 | FDA UDI | Class I | Active |
| Nar | 80-1503 | FDA UDI | N/A | Active |
| NAR Kit | 85-1752 | FDA UDI | N/A | Active |
| Nar | 84-0016 | FDA UDI | N/A | Active |
| Nar | 80-1705 | FDA UDI | Class I | Active |
| Nar | 80-1426 | FDA UDI | N/A | Active |
| Nar | 85-2059 | FDA UDI | N/A | Active |
| Nar | 80-1099 | FDA UDI | N/A | Active |
| Nar | 85-2517 | FDA UDI | N/A | Active |
| NAR Kit | 85-3808 | FDA UDI | N/A | Active |
| Nar | 85-1734 | FDA UDI | N/A | Active |
| Nar | 85-4297 | FDA UDI | Class I | Active |
| Nar | 85-4181 | FDA UDI | N/A | Active |
| Nar | 10-0001 | FDA UDI | Class I | Active |
| Nar | 85-4276 | FDA UDI | Class I | Active |
| NAR Kit | 82-0051 | FDA UDI | N/A | Active |
| Nar | 85-2508 | FDA UDI | N/A | Unknown |
| Nar | 85-3090 | FDA UDI | N/A | Active |
| NAR Kit | 80-1204 | FDA UDI | N/A | Active |
Related Companies
Authorised Representatives
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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 |