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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
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- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 5 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-3630 | FDA UDI | N/A | Active |
| Nar | 77-0102 | FDA UDI | Class I | Active |
| Nar | 84-0169 | FDA UDI | Class I | Active |
| Nar | 85-3884 | FDA UDI | N/A | Active |
| Nar | 85-2580 | FDA UDI | N/A | Active |
| Nar | 85-0177 | FDA UDI | N/A | Active |
| NAR Kit | 85-2950 | FDA UDI | N/A | Active |
| Nar | 82-0059 | FDA UDI | N/A | Active |
| Nar | 85-3689 | FDA UDI | N/A | Active |
| Nar | 85-3657 | FDA UDI | N/A | Active |
| NAR Kit | 85-0969 | FDA UDI | N/A | Active |
| NAR Kit | 85-2018 | FDA UDI | N/A | Active |
| Nar | 85-2779 | FDA UDI | N/A | Unknown |
| Nar | 85-3860 | FDA UDI | N/A | Active |
| Nar | 85-3043 | FDA UDI | N/A | Active |
| Nar | 85-1102 | FDA UDI | N/A | Active |
| NAR Kit | 80-1201 | FDA UDI | N/A | Active |
| NAR Kit | ZZ-0422 | FDA UDI | N/A | Active |
| NAR Kit | 85-2607 | FDA UDI | N/A | Active |
| Nar | 85-1770 | FDA UDI | N/A | Active |
| NAR Kit | 85-0016 | FDA UDI | N/A | Unknown |
| Nar | 84-0028 | FDA UDI | N/A | Active |
| Nar | 85-3589 | FDA UDI | N/A | Active |
| NAR Kit | 80-0375 | FDA UDI | N/A | Active |
| Nar | 85-4133 | FDA UDI | Class I | Active |
| Nar | 30-0093 | FDA UDI | Class I | Active |
| NAR Kit | 80-0948 | FDA UDI | N/A | Active |
| Nar | 82-0066 | FDA UDI | N | Active |
| Nar | 80-1537 | FDA UDI | N/A | Active |
| Nar | 85-4222 | FDA UDI | Class II | Active |
| Nar | ZZ-1036 | FDA UDI | Class I | Active |
| NAR Kit | 80-0384 | FDA UDI | N/A | Active |
| Nar | 85-2822 | FDA UDI | N/A | Active |
| Nar | 80-0870 | FDA UDI | N/A | Active |
| NAR Kit | 85-3026 | FDA UDI | N/A | Active |
| Nar | 85-3916 | FDA UDI | N/A | Active |
| Nar | 85-0355 | FDA UDI | N/A | Active |
| Nar | 85-2118 | FDA UDI | N/A | Active |
| Nar | 85-4010 | FDA UDI | N/A | Active |
| Nar | 85-4322 | FDA UDI | Class I | Active |
| Nar | 80-1423 | FDA UDI | N/A | Active |
| NAR Kit | 80-1232 | FDA UDI | N/A | Active |
| Nar | 85-2470 | FDA UDI | N/A | Active |
| Nar | 85-3354 | FDA UDI | N/A | Active |
| Nar | 85-4303 | FDA UDI | Class I | Active |
| Nar | 85-0634 | FDA UDI | N/A | Active |
| Nar | 85-3363 | FDA UDI | N/A | Active |
| Nar | 80-1452 | FDA UDI | Class I | Active |
| Nar | 85-4208 | FDA UDI | N/A | Active |
| Nar | 85-4432 | FDA UDI | Class I | 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 |