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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 28 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-4769 | FDA UDI | Class II | Active |
| Nar | 85-4873 | FDA UDI | Class I | Active |
| Nar | 80-1438 | FDA UDI | N/A | Active |
| Nar | 85-2709 | FDA UDI | N/A | Active |
| Nar | 80-0866 | FDA UDI | N/A | Active |
| Nar | 85-3901 | FDA UDI | N/A | Active |
| Nar | 85-3694 | FDA UDI | N/A | Active |
| Nar | 80-1056 | FDA UDI | N/A | Active |
| Nar | 85-2807 | FDA UDI | N/A | Active |
| Nar | 85-4374 | FDA UDI | Class I | Active |
| Nar | 85-3970 | FDA UDI | Class I | Active |
| Nar | 85-3911 | FDA UDI | N/A | Active |
| Nar | 83-0023 | FDA UDI | N/A | Active |
| Nar | 80-0469 | FDA UDI | N/A | Active |
| Nar | 80-1720 | FDA UDI | Class I | Active |
| NAR Kit | 85-1339 | FDA UDI | N/A | Active |
| Nar | 80-1495 | FDA UDI | N/A | Active |
| Nar | 80-1432 | FDA UDI | N/A | Active |
| Nar | 85-3097 | FDA UDI | N/A | Active |
| Nar | 85-3316 | FDA UDI | N/A | Active |
| NAR Kit | 85-0034 | FDA UDI | N/A | Active |
| NAR Kit | 10-0025 | FDA UDI | Class I | Active |
| Nar | 85-2587 | FDA UDI | N/A | Active |
| Nar | 84-0014 | FDA UDI | N/A | Active |
| Nar | 85-3011 | FDA UDI | N/A | Active |
| Nar | 85-0904 | FDA UDI | N/A | Active |
| Nar | 85-1980 | FDA UDI | N/A | Active |
| Nar | 80-1498 | FDA UDI | N/A | Active |
| Nar | 85-3165 | FDA UDI | N/A | Active |
| Nar | 80-1683 | FDA UDI | Class I | Active |
| Nar | 85-1554 | FDA UDI | N/A | Active |
| NAR Kit | 85-2655 | FDA UDI | N/A | Active |
| Nar | 85-4289 | FDA UDI | Class I | Active |
| Nar | 80-1851 | FDA UDI | Class II | Active |
| Nar | 85-2869 | FDA UDI | N/A | Active |
| Nar | 85-2742 | FDA UDI | N/A | Active |
| Nar | 85-1481 | FDA UDI | N/A | Active |
| NAR Kit | 85-0550 | FDA UDI | N/A | Active |
| Nar | 80-1505 | FDA UDI | N/A | Active |
| Nar | 85-3941 | FDA UDI | N/A | Active |
| Nar | 88-0010 | FDA UDI | Class I | Active |
| Nar | 85-4548 | FDA UDI | Class I | Active |
| Nar | 85-3968 | FDA UDI | N/A | Active |
| Sharps container | 30-0014 | FDA UDI | Class II | Active |
| Nar | 80-1807 | FDA UDI | N | Active |
| Nar | 80-1030 | FDA UDI | N/A | Active |
| Nar | 88-0020 | FDA UDI | Class I | Active |
| Nar | 85-4893 | FDA UDI | Class I | Active |
| NAR Kit | 85-3119 | FDA UDI | N/A | Active |
| Nar | 85-4072 | FDA UDI | N/A | 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 |