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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 52 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-4612 | FDA UDI | Class I | Active |
| NAR Kit | 85-1428 | FDA UDI | N/A | Active |
| NAR Kit | 80-0305 | FDA UDI | N/A | Unknown |
| Nar | 85-4100 | FDA UDI | N/A | Active |
| NAR Kit | 85-3379 | FDA UDI | N/A | Active |
| NAR Kit | 85-1034 | FDA UDI | N/A | Active |
| NAR Kit | 85-2795 | FDA UDI | N/A | Active |
| NAR Kit | 80-0383 | FDA UDI | N/A | Unknown |
| Nar | 85-2873 | FDA UDI | N/A | Active |
| Nar | 85-2656 | FDA UDI | N/A | Active |
| Nar | 85-4011 | FDA UDI | N/A | Active |
| Nar | 85-1603 | FDA UDI | N/A | Active |
| Nar | 85-4486 | FDA UDI | Class I | Active |
| Nar | 85-4915 | FDA UDI | Class I | Active |
| Nar | 85-3459 | FDA UDI | N/A | Active |
| Nar | 80-1732 | FDA UDI | Class I | Active |
| Nar | 77-0099 | FDA UDI | Class I | Active |
| Nar | 85-4188 | FDA UDI | N/A | Active |
| NAR Kit | 85-3189 | FDA UDI | N/A | Active |
| Nar | 85-4108 | FDA UDI | N/A | Active |
| Nar | 85-3254 | FDA UDI | N/A | Active |
| Nar | 85-2427 | FDA UDI | N/A | Active |
| Nar | 80-1442 | FDA UDI | N | Active |
| Nar | 80-1791 | FDA UDI | N | Active |
| Nar | 85-4593 | FDA UDI | Class I | Active |
| Nar | 30-0168 | FDA UDI | Class I | Active |
| Nar | 85-3600 | FDA UDI | N/A | Active |
| Nar | 80-1468 | FDA UDI | N/A | Active |
| Nar | 85-3160 | FDA UDI | N/A | Active |
| Nar | 85-4463 | FDA UDI | N | Active |
| NAR Kit | 70-0206 | FDA UDI | N/A | Active |
| Nar | 85-3648 | FDA UDI | Class I | Active |
| NAR Kit | 85-0753 | FDA UDI | N/A | Unknown |
| Nar | 85-3167 | FDA UDI | N/A | Active |
| Nar | 85-4581 | FDA UDI | Class I | Active |
| NAR Kit | 80-1145 | FDA UDI | N/A | Active |
| Nar | 85-4474 | FDA UDI | Class I | Active |
| Nar | 85-0925 | FDA UDI | N/A | Active |
| Nar | 85-4027 | FDA UDI | N/A | Active |
| Nar | 85-2831 | FDA UDI | N/A | Active |
| Nar | 77-0091 | FDA UDI | Class I | Active |
| Nar | 85-3664 | FDA UDI | N/A | Active |
| NAR Kit | 85-1449 | FDA UDI | N/A | Active |
| Nar | 85-3009 | FDA UDI | N/A | Active |
| Nar | 85-4603 | FDA UDI | N | Active |
| Nar | 80-1735 | FDA UDI | Class I | Active |
| Nar | 80-1491 | FDA UDI | N/A | Active |
| Nar | 85-2144 | FDA UDI | N/A | Active |
| Nar | 85-1868 | FDA UDI | N/A | Active |
| NAR Kit | 85-3489 | 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 |