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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 56 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-2730 | FDA UDI | N/A | Active |
| Nar | 83-0015 | FDA UDI | Class II | Active |
| Nar | 85-4628 | FDA UDI | Class I | Active |
| Nar | 85-4960 | FDA UDI | N | Active |
| Nar | 85-1535 | FDA UDI | N/A | Active |
| NAR Kit | 85-2949 | FDA UDI | N/A | Active |
| NAR Kit | 80-0072 | FDA UDI | N/A | Active |
| NAR Kit | 85-1162 | FDA UDI | Class II | Active |
| NAR Kit | 80-0210 | FDA UDI | N/A | Unknown |
| Nar | 85-0729 | FDA UDI | N/A | Active |
| Nar | 85-3001 | FDA UDI | N/A | Active |
| Nar | 85-3166 | FDA UDI | N/A | Active |
| Nar | 83-0022 | FDA UDI | Class II | Active |
| Nar | 85-3879 | FDA UDI | N/A | Active |
| Nar | 80-1661 | FDA UDI | Class I | Active |
| NAR Kit | 85-1381 | FDA UDI | N/A | Active |
| Nar | 85-2170 | FDA UDI | N/A | Active |
| Nar | 85-4519 | FDA UDI | N | Active |
| Nar | 80-1434 | FDA UDI | N/A | Active |
| Nar | 85-3617 | FDA UDI | N/A | Active |
| Nar | 10-0064 | FDA UDI | Class I | Active |
| Nar | 85-3907 | FDA UDI | N/A | Active |
| Nar | 80-1511 | FDA UDI | Class I | Active |
| Nar | 85-1523 | FDA UDI | N/A | Active |
| Nar | 85-4003 | FDA UDI | Class I | Active |
| NAR Kit | 85-1311 | FDA UDI | N/A | Active |
| NAR Kit | 80-0296 | FDA UDI | N/A | Unknown |
| NAR Kit | 85-2760 | FDA UDI | N/A | Active |
| Nar | 85-4648 | FDA UDI | Class I | Active |
| Nar | 80-1633 | FDA UDI | Class I | Active |
| Nar | 80-1821 | FDA UDI | N | Active |
| Nar | 80-1458 | FDA UDI | Class I | Active |
| Nar | 85-2217 | FDA UDI | N/A | Active |
| NAR Kit | 85-3447 | FDA UDI | N/A | Active |
| Nar | 85-3080 | FDA UDI | N/A | Active |
| Nar | 85-4219 | FDA UDI | N/A | Active |
| Nar | 85-4162 | FDA UDI | N/A | Active |
| Nar | 85-0973 | FDA UDI | N/A | Active |
| Nar | 84-0103 | FDA UDI | N/A | Active |
| NAR Kit | 80-1126 | FDA UDI | N/A | Active |
| Nar | 80-0167 | FDA UDI | N/A | Active |
| Nar | 80-0581 | FDA UDI | N/A | Active |
| Nar | 85-4284 | FDA UDI | Class II | Active |
| Nar | 85-2518 | FDA UDI | N/A | Active |
| Nar | 85-3064 | FDA UDI | N/A | Active |
| NAR Kit | 80-0284 | FDA UDI | N/A | Active |
| Nar | 85-2551 | FDA UDI | N/A | Active |
| Nar | 85-3857 | FDA UDI | N/A | Active |
| Nar | 85-3756 | FDA UDI | N/A | Active |
| NAR Kit | 85-1857 | FDA UDI | N/A | Active |
Related Companies
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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 |