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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 47 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-2995 | FDA UDI | N/A | Active |
| NAR Kit | 85-3725 | FDA UDI | N/A | Active |
| Nar | 83-0024 | FDA UDI | Class II | Active |
| NAR Kit | 80-0046 | FDA UDI | N/A | Active |
| Nar | 85-1485 | FDA UDI | Class I | Active |
| Nar | 85-4326 | FDA UDI | Class I | Active |
| Nar | 85-4757 | FDA UDI | Class I | Active |
| TACTICAL CricKIT | 85-2490 | FDA UDI | Class II | Active |
| Nar | 85-3839 | FDA UDI | N/A | Active |
| Nar | 85-4872 | FDA UDI | Class I | Active |
| NAR Kit | 85-3058 | FDA UDI | N/A | Active |
| Nar | 85-4705 | FDA UDI | Class I | Active |
| Nar | 85-1245 | FDA UDI | N/A | Active |
| Nar | 85-4462 | FDA UDI | Class I | Active |
| NAR Kit | 85-0457 | FDA UDI | N/A | Active |
| Nar | 77-0088 | FDA UDI | N | Active |
| Nar | 80-1106 | FDA UDI | N/A | Active |
| Nar | 85-2286 | FDA UDI | N/A | Active |
| NAR Kit | 85-1899 | FDA UDI | N/A | Active |
| NAR Kit | 85-3225 | FDA UDI | N/A | Active |
| Nar | 85-1293 | FDA UDI | N/A | Active |
| Nar | 30-0165 | FDA UDI | Class I | Active |
| NAR Kit | 80-0365 | FDA UDI | N/A | Unknown |
| Nar | 85-3450 | FDA UDI | N/A | Active |
| Nar | 85-3586 | FDA UDI | N/A | Active |
| Nar | 80-1625 | FDA UDI | Class I | Active |
| NAR Kit | 85-3158 | FDA UDI | N/A | Active |
| Nar | 80-1053 | FDA UDI | N/A | Active |
| NAR Kit | 85-0831 | FDA UDI | N/A | Active |
| Nar | 80-1699 | FDA UDI | Class I | Active |
| Nar | 85-3484 | FDA UDI | N/A | Active |
| NAR Kit | 85-3409 | FDA UDI | N/A | Active |
| Nar | 85-4018 | FDA UDI | N/A | Active |
| Nar | 85-3170 | FDA UDI | N/A | Active |
| NAR Kit | 85-3274 | FDA UDI | N/A | Active |
| Nar | 85-4103 | FDA UDI | N/A | Active |
| Nar | 85-4257 | FDA UDI | N | Active |
| Nar | 82-0042 | FDA UDI | N/A | Active |
| Nar | 85-3018 | FDA UDI | N/A | Active |
| Nar | 80-1084 | FDA UDI | N/A | Active |
| Nar | 85-3418 | FDA UDI | N/A | Active |
| Nar | 84-0171 | FDA UDI | Class I | Active |
| Nar | 80-1733 | FDA UDI | Class I | Active |
| Nar | 85-4059 | FDA UDI | N/A | Active |
| Nar | 85-3060 | FDA UDI | N/A | Active |
| NAR Kit | 80-0986 | FDA UDI | N/A | Active |
| NAR Kit | 85-2191 | FDA UDI | N/A | Active |
| Nar | 88-0008 | FDA UDI | Class I | Active |
| Nar | 85-3660 | FDA UDI | N/A | Active |
| Nar | 85-2973 | FDA UDI | N/A | Active |
Related Companies
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Importers
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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 |