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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 62 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-0509 | FDA UDI | N/A | Active |
| NAR Kit | 80-0117 | FDA UDI | N/A | Active |
| NAR Kit | 85-2827 | FDA UDI | N/A | Active |
| Nar | 85-2909 | FDA UDI | N/A | Active |
| NAR Kit | 85-2241 | FDA UDI | N/A | Active |
| NAR Kit | 85-2097 | FDA UDI | N/A | Active |
| Nar | 85-1816 | FDA UDI | N/A | Active |
| Nar | 85-1801 | FDA UDI | N/A | Active |
| Nar | 85-4121 | FDA UDI | N/A | Active |
| Nar | 85-1786 | FDA UDI | N/A | Active |
| Nar | 85-4277 | FDA UDI | Class I | Active |
| Nar | 85-2596 | FDA UDI | N/A | Active |
| Nar | 85-1785 | FDA UDI | N/A | Active |
| NAR kit | 84-0009 | FDA UDI | N/A | Active |
| Nar | 85-2734 | FDA UDI | N/A | Active |
| Nar | ZZ-0070 | FDA UDI | Class II | Unknown |
| Nar | 80-1178 | FDA UDI | N/A | Active |
| Nar | 85-2228 | FDA UDI | N/A | Active |
| Nar | 85-1608 | FDA UDI | N/A | Active |
| Nar | 85-3553 | FDA UDI | N/A | Active |
| NAR Kit | 85-0862 | FDA UDI | N/A | Unknown |
| Nar | 85-0404 | FDA UDI | N/A | Active |
| Nar | 85-2764 | FDA UDI | N/A | Active |
| NAR Kit | 80-0133 | FDA UDI | N/A | Active |
| NAR Kit | 85-1457 | FDA UDI | N/A | Active |
| NAR Kit | 85-1878 | FDA UDI | N/A | Unknown |
| Nar | ZZ-1450 | FDA UDI | N/A | Active |
| Nar | 85-4524 | FDA UDI | Class I | Active |
| Nar | 85-3794 | FDA UDI | N/A | Active |
| NAR Kit | 85-3563 | FDA UDI | N/A | Active |
| Nar | 85-2899 | FDA UDI | N/A | Active |
| Nar | 85-2844 | FDA UDI | N/A | Active |
| Nar | 85-1654 | FDA UDI | N/A | Active |
| NAR Kit | 80-0300 | FDA UDI | N/A | Active |
| Nar | 85-3590 | FDA UDI | N/A | Active |
| NAR Kit | 85-2763 | FDA UDI | N/A | Active |
| Nar | 85-3002 | FDA UDI | N/A | Active |
| NAR Kit | 80-1071 | FDA UDI | N/A | Active |
| Nar | 85-2723 | FDA UDI | N/A | Active |
| NAR Kit | 85-1410 | FDA UDI | N/A | Active |
| NAR Kit | 80-0175 | FDA UDI | N/A | Active |
| Nar | 85-1407 | FDA UDI | Class I | Active |
| NAR Kit | 85-1705 | FDA UDI | N/A | Active |
| Nar | 80-0526 | FDA UDI | N/A | Active |
| Nar | 82-0039 | FDA UDI | N/A | Active |
| Nar | 85-4224 | FDA UDI | N/A | Active |
| NAR Kit | 83-0009 | FDA UDI | N/A | Active |
| Nar | 85-4584 | FDA UDI | Class I | Active |
| Nar | 80-1192 | FDA UDI | N/A | Active |
| NAR Kit | 85-1839 | 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 |