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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 38 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 80-0467 | FDA UDI | N/A | Active |
| NAR Kit | 85-0520 | FDA UDI | N/A | Active |
| Nar | 85-4956 | FDA UDI | Class I | Active |
| Nar | 85-1817 | FDA UDI | N/A | Active |
| Nar | 85-4832 | FDA UDI | Class I | Active |
| Nar | 85-4174 | FDA UDI | N/A | Active |
| Nar | 85-1713 | FDA UDI | N/A | Active |
| Nar | 85-4549 | FDA UDI | N | Active |
| Nar | 85-3405 | FDA UDI | N/A | Active |
| NAR Kit | 85-0903 | FDA UDI | N/A | Active |
| NAR Kit | 85-1255 | FDA UDI | N/A | Active |
| Nar | 85-4074 | FDA UDI | N/A | Active |
| Nar | 80-1709 | FDA UDI | Class I | Active |
| Nar | 85-3697 | FDA UDI | N/A | Active |
| Nar | 85-4565 | FDA UDI | Class I | Active |
| NAR Kit | 85-1319 | FDA UDI | N/A | Active |
| Nar | 85-3611 | FDA UDI | N/A | Active |
| Nar | 85-3476 | FDA UDI | N/A | Active |
| NAR Kit | 85-1448 | FDA UDI | N/A | Active |
| NAR Kit | 85-0746 | FDA UDI | N/A | Active |
| Nar | 85-1490 | FDA UDI | N/A | Active |
| Nar | 85-3479 | FDA UDI | N/A | Active |
| Nar | 85-2955 | FDA UDI | N/A | Active |
| NAR Kit | 85-3244 | FDA UDI | N/A | Active |
| NAR kit | 84-0006 | FDA UDI | N/A | Active |
| Nar | 85-4680 | FDA UDI | Class I | Active |
| Nar | 85-2104 | FDA UDI | N/A | Active |
| Nar | 85-4457 | FDA UDI | Class I | Active |
| Nar | 85-2629 | FDA UDI | N/A | Active |
| Nar | 84-0179 | FDA UDI | Class I | Active |
| Nar | 80-1440 | FDA UDI | N/A | Active |
| Nar | 85-3163 | FDA UDI | N/A | Active |
| Nar | 85-1622 | FDA UDI | N/A | Active |
| NAR Kit | 85-1599 | FDA UDI | N/A | Unknown |
| Nar | 85-1623 | FDA UDI | N/A | Active |
| Nar | 85-4815 | FDA UDI | N | Active |
| Nar | 85-3882 | FDA UDI | N/A | Active |
| Nar | 80-1108 | FDA UDI | N/A | Active |
| NAR Kit | 85-2420 | FDA UDI | N/A | Active |
| NAR Kit | 80-1156 | FDA UDI | N/A | Active |
| NAR Kit | 85-2527 | FDA UDI | N/A | Active |
| Nar | 85-4745 | FDA UDI | Class I | Active |
| Nar | 85-4040 | FDA UDI | N/A | Active |
| Nar | 77-0103 | FDA UDI | Class I | Active |
| Nar | 85-3938 | FDA UDI | N/A | Active |
| NAR Kit | 85-3180 | FDA UDI | N/A | Active |
| Nar | 85-1578 | FDA UDI | N/A | Active |
| Nar | 85-3652 | FDA UDI | N/A | Active |
| Nar | 85-4679 | FDA UDI | Class I | Active |
| Nar | 85-1193 | 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 |