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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 7 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-0878 | FDA UDI | N/A | Active |
| Nar | 85-3645 | FDA UDI | N/A | Active |
| Nar | 85-2981 | FDA UDI | N/A | Active |
| Nar | 85-3560 | FDA UDI | N/A | Active |
| NAR Kit | 85-0964 | FDA UDI | N/A | Active |
| Nar | 85-4344 | FDA UDI | Class I | Active |
| NAR Kit | 85-0682 | FDA UDI | N/A | Active |
| NAR Kit | 80-1044 | FDA UDI | N/A | Active |
| Nar | 85-4368 | FDA UDI | Class I | Active |
| Nar | 85-4439 | FDA UDI | Class I | Active |
| Nar | 85-1545 | FDA UDI | N/A | Active |
| Nar | 85-3999 | FDA UDI | N/A | Active |
| Nar | 84-0166 | FDA UDI | Class I | Active |
| Nar | 85-4746 | FDA UDI | Class I | Active |
| Nar | 85-4912 | FDA UDI | Class I | Active |
| Nar | 85-1849 | FDA UDI | N/A | Active |
| Nar | 85-4047 | FDA UDI | N/A | Active |
| NAR Kit | 85-1469 | FDA UDI | N/A | Active |
| Nar | 85-1367 | FDA UDI | N/A | Active |
| NAR Kit | 85-1742 | FDA UDI | N/A | Active |
| NAR Kit | 85-1615 | FDA UDI | N/A | Active |
| NAR Kit | 80-1068 | FDA UDI | N/A | Active |
| Nar | 80-1206 | FDA UDI | N/A | Active |
| NAR Kit | 85-1644 | FDA UDI | N/A | Active |
| NAR Kit | 30-0013 | FDA UDI | Class II | Active |
| Nar | 84-0163 | FDA UDI | Class I | Active |
| Nar | 85-2688 | FDA UDI | N/A | Active |
| Nar | 85-4936 | FDA UDI | Class I | Active |
| Nar | 85-2279 | FDA UDI | N/A | Active |
| NAR Kit | 85-1530 | FDA UDI | N/A | Active |
| Nar | 85-4573 | FDA UDI | Class I | Active |
| NAR Kit | 85-3693 | FDA UDI | N/A | Active |
| Nar | 60-0027 | FDA UDI | Class I | Active |
| NAR Kit | 80-0060 | FDA UDI | N/A | Active |
| NAR Kit | 80-1005 | FDA UDI | N/A | Active |
| Nar | 85-2338 | FDA UDI | N/A | Active |
| Nar | 85-0018 | FDA UDI | N/A | Active |
| Nar | 85-3512 | FDA UDI | N/A | Active |
| NAR Kit | 85-0519 | FDA UDI | N/A | Active |
| Nar | 85-3473 | FDA UDI | N/A | Active |
| Nar | 85-3776 | FDA UDI | N/A | Active |
| NAR Kit | 85-1806 | FDA UDI | N/A | Active |
| Nar | 85-2962 | FDA UDI | N/A | Active |
| Nar | 85-4167 | FDA UDI | Class I | Active |
| Nar | 85-4009 | FDA UDI | N/A | Active |
| NAR Kit | 80-1091 | FDA UDI | N/A | Active |
| Nar | 85-3190 | FDA UDI | N/A | Active |
| Nar | 84-0165 | FDA UDI | Class I | Active |
| Nar | 85-4128 | FDA UDI | N/A | Active |
| Nar | 82-0085 | FDA UDI | N | 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 |