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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 1 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-0865 | FDA UDI | N/A | Active |
| Nar | 80-1138 | FDA UDI | N/A | Active |
| Nar | 80-1686 | FDA UDI | Class I | Active |
| Nar | 85-1586 | FDA UDI | Class I | Active |
| Nar | 85-4068 | FDA UDI | N/A | Active |
| Nar | 85-3978 | FDA UDI | N/A | Active |
| Nar | 85-3339 | FDA UDI | N/A | Active |
| NAR Kit | 85-3414 | FDA UDI | N/A | Active |
| Nar | 85-4692 | FDA UDI | Class I | Active |
| Nar | 85-3935 | FDA UDI | N/A | Active |
| Nar | 85-2149 | FDA UDI | N/A | Active |
| Nar | 85-2114 | FDA UDI | N/A | Active |
| NAR Kit | 85-1842 | FDA UDI | N/A | Active |
| Nar | 85-3829 | FDA UDI | N/A | Active |
| Nar | 85-4810 | FDA UDI | Class I | Active |
| NAR Kit | 85-2778 | FDA UDI | N/A | Active |
| Nar | 85-3120 | FDA UDI | N/A | Active |
| Nar | 85-2714 | FDA UDI | N/A | Active |
| Nar | 85-2811 | FDA UDI | N/A | Active |
| NAR Kit | 85-2256 | FDA UDI | N/A | Active |
| Nar | 85-2080 | FDA UDI | N/A | Active |
| Nar | 80-0583 | FDA UDI | N/A | Active |
| Nar | 85-1620 | FDA UDI | N/A | Active |
| Nar | 85-4630 | FDA UDI | Class I | Active |
| Nar | 83-0002 | FDA UDI | Class II | Active |
| Nar | 85-4442 | FDA UDI | Class I | Active |
| Nar | 85-3150 | FDA UDI | N/A | Active |
| Nar | 83-0039 | FDA UDI | Class I | Active |
| Nar | 85-4392 | FDA UDI | Class I | Active |
| NAR Kit | 85-3416 | FDA UDI | N/A | Active |
| NAR Kit | 85-1145 | FDA UDI | N/A | Active |
| Nar | 80-0497 | FDA UDI | N/A | Active |
| Nar | 85-2917 | FDA UDI | N/A | Active |
| Nar | 85-1974 | FDA UDI | N/A | Active |
| Nar | 85-4305 | FDA UDI | Class I | Active |
| Nar | 85-2466 | FDA UDI | N/A | Active |
| NAR Kit | 85-3032 | FDA UDI | N/A | Active |
| NAR Kit | 85-2103 | FDA UDI | N/A | Active |
| Nar | 85-1044 | FDA UDI | N/A | Active |
| Nar | 85-4186 | FDA UDI | N/A | Active |
| NAR Kit | 85-1306 | FDA UDI | N/A | Active |
| NAR Kit | 70-0216 | FDA UDI | N/A | Active |
| Nar | 85-1246 | FDA UDI | N/A | Active |
| Nar | 85-1331 | FDA UDI | N/A | Active |
| Nar | 85-3821 | FDA UDI | N/A | Active |
| Nar | 85-4579 | FDA UDI | Class I | Active |
| Nar | 85-3427 | FDA UDI | Class I | Active |
| NAR Kit | 85-2568 | FDA UDI | N/A | Active |
| Nar | 80-1594 | FDA UDI | N | Active |
| Nar | 85-4265 | FDA UDI | Class I | 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 |