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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 42 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-1097 | FDA UDI | N/A | Active |
| Nar | 85-4488 | FDA UDI | Class I | Active |
| Nar | 85-3951 | FDA UDI | N/A | Active |
| Nar | 85-4751 | FDA UDI | Class I | Active |
| NAR Kit | 85-2295 | FDA UDI | N/A | Active |
| Nar | 85-1359 | FDA UDI | N/A | Active |
| Nar | 85-2732 | FDA UDI | N/A | Active |
| NAR Kit | 82-0032 | FDA UDI | N/A | Unknown |
| Nar | 77-0085 | FDA UDI | Class I | Active |
| NAR Kit | 85-1970 | FDA UDI | N/A | Active |
| Nar | 85-4765 | FDA UDI | Class I | Active |
| Nar | 77-0084 | FDA UDI | Class I | Active |
| Nar | 85-4017 | FDA UDI | N/A | Active |
| Nar | 85-4510 | FDA UDI | Class I | Active |
| NAR Kit | 85-2093 | FDA UDI | N/A | Active |
| Nar | 85-4049 | FDA UDI | N/A | Active |
| Nar | 85-4806 | FDA UDI | Class I | Active |
| Nar | 77-0089 | FDA UDI | Class I | Active |
| Nar | 85-3878 | FDA UDI | N/A | Active |
| Nar | 80-1173 | FDA UDI | N/A | Active |
| Nar | 85-1995 | FDA UDI | N/A | Active |
| NAR Kit | 80-0457 | FDA UDI | N/A | Active |
| Nar | 85-4917 | FDA UDI | Class I | Active |
| Nar | 84-0146 | FDA UDI | Class I | Active |
| Nar | 80-0353 | FDA UDI | N/A | Active |
| NAR Kit | 85-2659 | FDA UDI | N/A | Active |
| NAR Kit | 85-3570 | FDA UDI | N/A | Active |
| Nar | 80-0890 | FDA UDI | N/A | Active |
| NAR Kit | 85-1678 | FDA UDI | N/A | Active |
| Nar | 85-3008 | FDA UDI | N/A | Active |
| NAR Kit | 85-1049 | FDA UDI | N/A | Active |
| NAR Kit | 85-3728 | FDA UDI | N/A | Active |
| Nar | 85-4667 | FDA UDI | Class I | Active |
| NAR Kit | 85-2594 | FDA UDI | N/A | Active |
| Nar | 85-2541 | FDA UDI | N/A | Active |
| Nar | 85-4498 | FDA UDI | Class I | Active |
| Nar | 85-3601 | FDA UDI | N/A | Active |
| Nar | 85-3533 | FDA UDI | N/A | Active |
| NAR Kit | 80-0301 | FDA UDI | N/A | Active |
| Nar | 85-1892 | FDA UDI | N/A | Active |
| Nar | 85-3773 | FDA UDI | N/A | Active |
| Nar | 85-3394 | FDA UDI | N/A | Active |
| Nar | 85-3659 | FDA UDI | N/A | Active |
| NAR Kit | 85-3564 | FDA UDI | N/A | Active |
| Nar | 85-4781 | FDA UDI | Class I | Active |
| Nar | 85-1702 | FDA UDI | N/A | Active |
| Nar | 85-4248 | FDA UDI | N/A | Active |
| Nar | 80-1007 | FDA UDI | N/A | Active |
| NAR Kit | 80-0418 | FDA UDI | N/A | Active |
| NAR Kit | 80-0294 | FDA UDI | N/A | Unknown |
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 |