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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 57 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-2838 | FDA UDI | N/A | Active |
| Nar | 85-2437 | FDA UDI | Class I | Active |
| NAR Kit | 85-3547 | FDA UDI | N/A | Active |
| Nar | 80-0940 | FDA UDI | N/A | Active |
| Nar | 85-1925 | FDA UDI | N/A | Active |
| Nar | 77-0075 | FDA UDI | Class I | Active |
| Nar | 85-3870 | FDA UDI | N/A | Active |
| Nar | 85-3122 | FDA UDI | N/A | Active |
| Nar | 80-0475 | FDA UDI | N/A | Active |
| NAR Kit | 85-2828 | FDA UDI | N/A | Active |
| Nar | 85-1577 | FDA UDI | N/A | Active |
| Nar | 80-1743 | FDA UDI | Class I | Active |
| Nar | 85-3896 | FDA UDI | N/A | Active |
| Nar | 85-4482 | FDA UDI | Class I | Active |
| Nar | 85-3581 | FDA UDI | N/A | Active |
| NAR Kit | 85-2774 | FDA UDI | N/A | Active |
| NAR Kit | 85-1519 | FDA UDI | N/A | Active |
| Nar | 85-3373 | FDA UDI | N/A | Active |
| NAR Kit | 84-0005 | FDA UDI | N/A | Active |
| Nar | 80-0960 | FDA UDI | N | Active |
| Nar | 85-3663 | FDA UDI | N/A | Active |
| Nar | 85-4364 | FDA UDI | Class I | Active |
| Nar | 85-1581 | FDA UDI | N/A | Active |
| Nar | 84-0101 | FDA UDI | N/A | Active |
| Nar | 85-2039 | FDA UDI | N/A | Active |
| Nar | 85-4869 | FDA UDI | N | Active |
| Nar | 85-3469 | FDA UDI | N/A | Active |
| Nar | 85-2562 | FDA UDI | N/A | Active |
| NAR Kit | 85-1351 | FDA UDI | N/A | Active |
| NAR Kit | 85-3248 | FDA UDI | N/A | Active |
| Nar | 85-1853 | FDA UDI | N/A | Active |
| Nar | 85-4056 | FDA UDI | N/A | Active |
| Nar | 85-2772 | FDA UDI | N/A | Active |
| Nar | 85-3641 | FDA UDI | N/A | Active |
| NAR Kit | 80-1033 | FDA UDI | N/A | Active |
| Nar | 30-0171 | FDA UDI | Class I | Active |
| Nar | 80-1104 | FDA UDI | N/A | Active |
| NAR Kit | 85-1435 | FDA UDI | N/A | Unknown |
| Nar | 85-2918 | FDA UDI | N/A | Active |
| Nar | 85-4286 | FDA UDI | Class I | Active |
| NAR Kit | 80-0517 | FDA UDI | N/A | Active |
| Nar | 85-4770 | FDA UDI | Class I | Active |
| Nar | 85-2071 | FDA UDI | N/A | Active |
| Nar | 85-2121 | FDA UDI | N/A | Active |
| Nar | 85-1386 | FDA UDI | N/A | Active |
| Nar | 85-1544 | FDA UDI | N/A | Active |
| Nar | 85-4255 | FDA UDI | N/A | Active |
| Nar | 85-4191 | FDA UDI | N/A | Active |
| NAR Kit | 85-3223 | FDA UDI | N/A | Active |
| Nar | 85-3332 | 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 |