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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 27 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-4200 | FDA UDI | N/A | Active |
| Nar | 85-3746 | FDA UDI | N/A | Active |
| Nar | 85-1975 | FDA UDI | Class I | Active |
| Nar | 85-2846 | FDA UDI | N/A | Active |
| Nar | 85-1717 | FDA UDI | N/A | Active |
| Nar | 85-1574 | FDA UDI | N/A | Active |
| Nar | 85-4529 | FDA UDI | Class I | Active |
| Nar | 80-1844 | FDA UDI | Class I | Active |
| Nar | 85-3940 | FDA UDI | N/A | Active |
| Nar | 85-4624 | FDA UDI | Class I | Active |
| Nar | 85-4823 | FDA UDI | N | Active |
| Nar | 80-1692 | FDA UDI | Class I | Active |
| Nar | 30-0307 | FDA UDI | N/A | Active |
| Nar | 35-0026 | FDA UDI | Class I | Active |
| Nar | 85-4639 | FDA UDI | Class I | Active |
| Nar | 85-3431 | FDA UDI | N/A | Active |
| Nar | 85-1993 | FDA UDI | N/A | Active |
| Nar | 85-1714 | FDA UDI | N/A | Active |
| Nar | 85-3628 | FDA UDI | N/A | Active |
| Nar | 85-1747 | FDA UDI | N/A | Active |
| NAR Kit | 85-1537 | FDA UDI | N/A | Active |
| Nar | 85-4595 | FDA UDI | Class I | Active |
| Nar | 80-1727 | FDA UDI | Class I | Active |
| NAR Kit | 85-3699 | FDA UDI | N/A | Active |
| Nar | 85-3025 | FDA UDI | N/A | Active |
| Nar | 80-1751 | FDA UDI | Class I | Active |
| Nar | 80-1689 | FDA UDI | Class I | Active |
| Nar | 85-3747 | FDA UDI | N/A | Active |
| NAR Kit | 85-2966 | FDA UDI | N/A | Active |
| Nar | 85-1746 | FDA UDI | N/A | Active |
| NAR Kit | 85-3185 | FDA UDI | N/A | Active |
| Nar | 85-4637 | FDA UDI | Class I | Active |
| Nar | 85-3638 | FDA UDI | N/A | Active |
| Nar | 85-2003 | FDA UDI | N/A | Active |
| Nar | 85-3834 | FDA UDI | N/A | Active |
| Nar | 85-0409 | FDA UDI | N/A | Active |
| Nar | 80-1731 | FDA UDI | Class I | Active |
| Nar | 85-4038 | FDA UDI | N/A | Active |
| Nar | 84-0099 | FDA UDI | N/A | Active |
| Nar | 85-2841 | FDA UDI | N/A | Active |
| Nar | 85-4632 | FDA UDI | Class I | Active |
| Nar | 80-1761 | FDA UDI | Class I | Active |
| Nar | 80-1137 | FDA UDI | N/A | Active |
| Nar | 85-0388 | FDA UDI | N/A | Active |
| Nar | 85-4509 | FDA UDI | Class I | Active |
| NAR Kit | 85-3742 | FDA UDI | N/A | Active |
| Nar | 85-0408 | FDA UDI | N/A | Active |
| NAR Kit | 80-1032 | FDA UDI | N/A | Active |
| NAR Kit | 85-0742 | FDA UDI | N/A | Active |
| Nar | 80-1554 | FDA UDI | Class I | Active |
Related Companies
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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 |