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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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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 18 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-2939 | FDA UDI | N/A | Active |
| Nar | 85-4813 | FDA UDI | Class I | Active |
| NAR Kit | 85-3302 | FDA UDI | N/A | Active |
| Nar | 80-1711 | FDA UDI | Class I | Active |
| Nar | 85-3176 | FDA UDI | N/A | Active |
| NAR Kit | 80-0921 | FDA UDI | N/A | Active |
| NAR Kit | 85-1461 | FDA UDI | N/A | Active |
| Nar | 80-1816 | FDA UDI | Class I | Active |
| NAR Kit | 85-3803 | FDA UDI | N/A | Active |
| NAR Kit | 84-0004 | FDA UDI | N/A | Active |
| Nar | 85-1607 | FDA UDI | N/A | Active |
| NAR Kit | 80-0209 | FDA UDI | N/A | Active |
| Nar | 80-1571 | FDA UDI | N/A | Active |
| Nar | 85-3800 | FDA UDI | N/A | Active |
| Nar | 85-3054 | FDA UDI | N/A | Active |
| NAR Kit | 85-2237 | FDA UDI | N/A | Active |
| TACTICAL CricKIT | 85-0291 | FDA UDI | Class II | Active |
| NAR Kit | 85-2329 | FDA UDI | N/A | Active |
| NAR Kit | 85-2564 | FDA UDI | N/A | Active |
| Nar | 85-4071 | FDA UDI | N/A | Active |
| NAR Kit | 80-1223 | FDA UDI | N/A | Active |
| Nar | 85-4231 | FDA UDI | N/A | Active |
| Nar | 80-1741 | FDA UDI | Class I | Active |
| Nar | 80-1424 | FDA UDI | N/A | Active |
| NAR Kit | 85-0984 | FDA UDI | N/A | Active |
| Nar | 80-1170 | FDA UDI | N/A | Active |
| Nar | 84-0154 | FDA UDI | Class I | Active |
| Nar | 80-1501 | FDA UDI | N/A | Active |
| Nar | 80-1480 | FDA UDI | N/A | Active |
| Nar | 85-3156 | FDA UDI | N/A | Active |
| Nar | 85-0701 | FDA UDI | N/A | Active |
| Nar | 85-3525 | FDA UDI | N/A | Active |
| Nar | 85-1774 | FDA UDI | N/A | Active |
| Nar | 85-3575 | FDA UDI | N/A | Active |
| Nar | 80-0869 | FDA UDI | N/A | Active |
| Nar | 85-2309 | FDA UDI | N/A | Active |
| NAR Kit | 85-2805 | FDA UDI | N/A | Active |
| Nar | 85-4926 | FDA UDI | Class I | Active |
| Nar | 85-4933 | FDA UDI | Class I | Active |
| NAR Kit | 85-0992 | FDA UDI | N/A | Active |
| Nar | 85-2733 | FDA UDI | N/A | Active |
| Nar | 85-2623 | FDA UDI | N/A | Active |
| Nar | 80-1839 | FDA UDI | Class I | Active |
| Nar | 85-3159 | FDA UDI | N/A | Active |
| Nar | 85-4107 | FDA UDI | N/A | Active |
| NAR Kit | 85-1267 | FDA UDI | N/A | Active |
| NAR Kit | 80-0406 | FDA UDI | N/A | Active |
| Nar | 85-1766 | FDA UDI | N/A | Active |
| Nar | 85-3754 | FDA UDI | N/A | Active |
| NAR Kit | 85-0842 | FDA UDI | N/A | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
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 |