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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 44 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-0923 | FDA UDI | N/A | Active |
| NAR Kit | 85-3259 | FDA UDI | N/A | Active |
| Nar | 85-2345 | FDA UDI | N/A | Active |
| NAR Kit | 85-3092 | FDA UDI | N/A | Active |
| Nar | 85-4671 | FDA UDI | Class I | Active |
| Nar | 85-4304 | FDA UDI | Class I | Active |
| Nar | 85-3633 | FDA UDI | N/A | Active |
| Nar | 85-4567 | FDA UDI | Class I | Active |
| Nar | 85-4621 | FDA UDI | Class I | Active |
| NAR Kit | 85-3094 | FDA UDI | N/A | Active |
| Nar | 85-1455 | FDA UDI | N/A | Active |
| Nar | 85-1112 | FDA UDI | Class I | Active |
| Nar | 85-4470 | FDA UDI | Class I | Active |
| NAR Kit | 80-0518 | FDA UDI | N/A | Active |
| Nar | 85-2717 | FDA UDI | Class I | Active |
| Nar | 80-1134 | FDA UDI | N/A | Active |
| Nar | 85-3053 | FDA UDI | N/A | Active |
| Nar | 30-0003 | FDA UDI | Class I | Active |
| Nar | 80-1128 | FDA UDI | N/A | Active |
| Nar | 85-2272 | FDA UDI | N/A | Active |
| Nar | 85-2182 | FDA UDI | N/A | Active |
| Nar | 85-3143 | FDA UDI | N/A | Active |
| Nar | 85-4045 | FDA UDI | N/A | Active |
| Nar | 85-2624 | FDA UDI | N/A | Active |
| Nar | 85-3086 | FDA UDI | N/A | Active |
| Nar | 85-4443 | FDA UDI | Class I | Active |
| NAR Kit | 85-2818 | FDA UDI | N/A | Active |
| NAR Kit | 85-2038 | FDA UDI | N/A | Active |
| Nar | 85-3724 | FDA UDI | N/A | Active |
| Nar | 80-1815 | FDA UDI | Class I | Active |
| Nar | 85-4164 | FDA UDI | N/A | Active |
| Nar | 85-3991 | FDA UDI | N/A | Active |
| Nar | 85-4205 | FDA UDI | N/A | Active |
| Nar | 85-3108 | FDA UDI | N/A | Active |
| Nar | 85-4424 | FDA UDI | Class I | Active |
| NAR Kit | 80-1034 | FDA UDI | N/A | Active |
| Nar | 85-3695 | FDA UDI | N/A | Active |
| Nar | 85-3688 | FDA UDI | N/A | Active |
| Nar | 85-4247 | FDA UDI | Class I | Active |
| NAR Kit | 85-1680 | FDA UDI | N/A | Active |
| Nar | 85-3435 | FDA UDI | Class I | Active |
| Nar | 80-1774 | FDA UDI | N | Active |
| Nar | 80-1460 | FDA UDI | N/A | Active |
| Nar | 85-4883 | FDA UDI | Class I | Active |
| Nar | 80-1422 | FDA UDI | Class I | Active |
| Nar | 30-0162 | FDA UDI | Class I | Active |
| Nar | 85-3529 | FDA UDI | N/A | Active |
| Nar | 85-2430 | FDA UDI | N/A | Active |
| Nar | 85-1978 | FDA UDI | N/A | Active |
| NAR Kit | 80-0203 | 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 |