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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 67 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-1584 | FDA UDI | N/A | Active |
| NAR Kit | 85-3355 | FDA UDI | N/A | Active |
| NAR Kit | 82-0034 | FDA UDI | N/A | Active |
| Nar | 30-0003 | FDA UDI | Class I | Active |
| NAR Kit | 80-0374 | FDA UDI | N/A | Active |
| Nar | 85-3456 | FDA UDI | N/A | Active |
| Nar | 85-4850 | FDA UDI | N | Active |
| Nar | 85-4273 | FDA UDI | N/A | Active |
| Nar | 80-0926 | FDA UDI | N/A | Active |
| Nar | 85-3898 | FDA UDI | N/A | Active |
| NAR Kit | 85-2154 | FDA UDI | N/A | Active |
| Nar | 85-2202 | FDA UDI | N/A | Active |
| Nar | 85-4727 | FDA UDI | Class I | Active |
| Nar | 85-2977 | FDA UDI | N/A | Active |
| Nar | 85-1903 | FDA UDI | N/A | Active |
| NAR Kit | 85-0967 | FDA UDI | N/A | Active |
| Nar | 85-3880 | FDA UDI | N/A | Active |
| Nar | 85-3433 | FDA UDI | Class I | Active |
| Nar | 85-3234 | FDA UDI | N/A | Active |
| Nar | 85-2129 | FDA UDI | N/A | Active |
| NAR Kit | 80-1151 | FDA UDI | N/A | Active |
| NAR Kit | 85-2835 | FDA UDI | N/A | Active |
| Nar | 85-3919 | FDA UDI | N/A | Active |
| NAR Kit | 85-1712 | FDA UDI | N/A | Active |
| NAR Kit | 85-1598 | FDA UDI | N/A | Active |
| Nar | 85-4562 | FDA UDI | Class I | Active |
| Nar | 85-3104 | FDA UDI | N/A | Active |
| Nar | 85-1741 | FDA UDI | N/A | Active |
| NAR Kit | 85-1953 | FDA UDI | N/A | Active |
| NAR Kit | ZZ-0387 | FDA UDI | N/A | Active |
| NAR Kit | 82-0000 | FDA UDI | N/A | Active |
| Black Talon | ZZ-0274 | FDA UDI | Class I | Active |
| Nar | 80-1729 | FDA UDI | Class I | Active |
| Nar | 30-0310 | FDA UDI | Class I | Active |
| Nar | 85-3671 | FDA UDI | N/A | Active |
| Nar | 85-2582 | FDA UDI | N/A | Active |
| NAR Cricothyrotomy Kit | 10-0048 | FDA UDI | Class II | Unknown |
| NAR Kit | 85-3047 | FDA UDI | N/A | Active |
| Nar | 85-2959 | FDA UDI | N/A | Active |
| Nar | 85-1316 | FDA UDI | N/A | Active |
| NAR Kit | ZZ-1176 | FDA UDI | N/A | Active |
| Nar | 85-2333 | FDA UDI | N/A | Active |
| Nar | 85-2686 | FDA UDI | N/A | Active |
| NAR Kit | 80-0443 | FDA UDI | N/A | Active |
| Nar | 85-3682 | FDA UDI | N/A | Active |
| Nar | 84-0090 | FDA UDI | N/A | Active |
| Nar | 85-3971 | FDA UDI | N/A | Active |
| NAR Kit | 82-0035 | FDA UDI | N/A | Active |
| Nar | 83-0028 | FDA UDI | Class II | Active |
| NAR Kit | 85-3260 | 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 |