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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 13 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-1701 | FDA UDI | Class I | Active |
| Nar | 85-4843 | FDA UDI | Class I | Active |
| Nar | 80-1737 | FDA UDI | Class I | Active |
| Nar | 80-1497 | FDA UDI | N/A | Active |
| Nar | 85-3961 | FDA UDI | N/A | Active |
| Nar | 85-4044 | FDA UDI | N/A | Active |
| Nar | 85-2342 | FDA UDI | N/A | Active |
| Nar | 80-0863 | FDA UDI | N/A | Active |
| Nar | 85-4325 | FDA UDI | Class I | Active |
| Nar | 85-4911 | FDA UDI | Class I | Active |
| Nar | 85-4537 | FDA UDI | Class I | Active |
| Nar | 85-3634 | FDA UDI | N/A | Active |
| Nar | 85-4602 | FDA UDI | N | Active |
| Nar | 85-3534 | FDA UDI | N/A | Active |
| NAR Kit | 80-0304 | FDA UDI | N/A | Unknown |
| NAR Kit | 85-2514 | FDA UDI | N/A | Active |
| Nar | 85-2360 | FDA UDI | N/A | Active |
| Nar | 85-4748 | FDA UDI | Class I | Active |
| Nar | 85-4957 | FDA UDI | Class I | Active |
| Nar | 85-3257 | FDA UDI | N/A | Active |
| Nar | 83-0021 | FDA UDI | N/A | Active |
| Nar | 85-3157 | FDA UDI | N/A | Active |
| Nar | 85-2255 | FDA UDI | N/A | Active |
| Nar | 85-3361 | FDA UDI | N/A | Active |
| Nar | 80-1578 | FDA UDI | Class I | Active |
| Nar | 85-2450 | FDA UDI | N/A | Active |
| NAR Kit | 85-2446 | FDA UDI | N/A | Active |
| Nar | 85-4029 | FDA UDI | N/A | Active |
| Nar | 85-4178 | FDA UDI | N/A | Active |
| NAR Kit | 80-1191 | FDA UDI | N/A | Active |
| NAR Kit | 85-2340 | FDA UDI | N/A | Active |
| NAR Kit | 85-2417 | FDA UDI | N/A | Active |
| Nar | 85-4213 | FDA UDI | Class I | Active |
| Nar | 85-3718 | FDA UDI | N/A | Active |
| NAR Kit | 80-0013 | FDA UDI | N/A | Active |
| NAR Kit | 85-1369 | FDA UDI | N/A | Active |
| NAR Kit | 85-1231 | FDA UDI | N/A | Unknown |
| Nar | 85-4798 | FDA UDI | N | Active |
| Nar | 80-1205 | FDA UDI | N/A | Active |
| NAR Kit | 85-1867 | FDA UDI | N/A | Active |
| Nar | 80-1663 | FDA UDI | Class I | Active |
| NAR Kit | 85-2922 | FDA UDI | N/A | Active |
| NAR Kit | 85-1626 | FDA UDI | N/A | Active |
| Nar | 80-1552 | FDA UDI | Class I | Active |
| Nar | 85-2444 | FDA UDI | N/A | Active |
| Nar | 85-3669 | FDA UDI | N/A | Active |
| Nar | 85-2769 | FDA UDI | N/A | Active |
| NAR Kit | 85-1138 | FDA UDI | N/A | Active |
| Nar | 80-1830 | FDA UDI | N | Active |
| Nar | 80-1592 | FDA UDI | N/A | Active |
Related Companies
Authorised Representatives
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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 |