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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 69 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 30-0031 | FDA UDI | Class I | Active |
| Nar | 80-1832 | FDA UDI | N | Active |
| Nar | 88-0016 | FDA UDI | Class I | Active |
| Nar | 85-3805 | FDA UDI | N/A | Active |
| Nar | 85-4589 | FDA UDI | Class I | Active |
| Nar | 85-2642 | FDA UDI | N/A | Active |
| NAR Kit | 85-1218 | FDA UDI | N/A | Active |
| Nar | 85-3683 | FDA UDI | N/A | Active |
| Nar | 85-3559 | FDA UDI | N/A | Active |
| NAR Kit | 85-2646 | FDA UDI | N/A | Active |
| Nar | 85-3678 | FDA UDI | N/A | Active |
| NAR Kit | 85-1111 | FDA UDI | N/A | Active |
| NAR Kit | 85-0639 | FDA UDI | N/A | Active |
| Nar | 85-2628 | FDA UDI | N/A | Active |
| NAR Kit | 80-0501 | FDA UDI | N/A | Active |
| Life Warmer Quantum Battery | 63-5902 | FDA UDI | Class II | Active |
| Nar | 85-2604 | FDA UDI | N/A | Active |
| NAR Kit | 85-0889 | FDA UDI | N/A | Active |
| Nar | 85-4270 | FDA UDI | Class I | Active |
| NAR Kit | 80-0320 | FDA UDI | N/A | Active |
| NAR Kit | 80-0442 | FDA UDI | N/A | Active |
| Nar | 85-4467 | FDA UDI | Class I | Active |
| Nar | 85-4811 | FDA UDI | Class I | Active |
| NAR Kit | 85-2100 | FDA UDI | N/A | Active |
| Nar | 85-3175 | FDA UDI | N/A | Active |
| NAR Kit | 85-1459 | FDA UDI | N/A | Active |
| Nar | 85-2816 | FDA UDI | N/A | Active |
| Nar | 85-2115 | FDA UDI | N/A | Active |
| Nar | 85-1749 | FDA UDI | N/A | Active |
| NAR Kit | 85-2290 | FDA UDI | Class II | Active |
| Nar | 85-4223 | FDA UDI | Class II | Active |
| Nar | 85-4921 | FDA UDI | Class I | Active |
| NAR Kit | 85-1444 | FDA UDI | N/A | Unknown |
| Nar | 85-2538 | FDA UDI | N/A | Active |
| Nar | 85-3308 | FDA UDI | N/A | Active |
| Nar | 83-0006 | FDA UDI | N/A | Active |
| Nar | 80-1696 | FDA UDI | Class I | Active |
| Nar | 82-0057 | FDA UDI | N/A | Active |
| Nar | 85-3837 | FDA UDI | N/A | Active |
| Nar | 84-0027 | FDA UDI | N/A | Active |
| NAR Kit | 85-1788 | FDA UDI | N/A | Active |
| Nar | 80-1534 | FDA UDI | Class I | Active |
| Nar | 85-4633 | FDA UDI | Class I | Active |
| NAR Kit | 85-1795 | FDA UDI | N/A | Active |
| Nar | 80-1749 | FDA UDI | Class I | Active |
| NAR Kit | 85-1254 | FDA UDI | N/A | Active |
| NAR Kit | 85-2405 | FDA UDI | N/A | Active |
| NAR Kit | 85-0309 | FDA UDI | N/A | Active |
| Nar | 80-1615 | FDA UDI | N | Active |
| NAR Kit | 80-0504 | 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 |