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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 39 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-2507 | FDA UDI | N/A | Active |
| NAR Kit | 85-1344 | FDA UDI | N/A | Active |
| Nar | 80-1715 | FDA UDI | Class I | Active |
| Nar | 85-2425 | FDA UDI | N/A | Active |
| Nar | 85-3088 | FDA UDI | N/A | Active |
| Nar | 80-1716 | FDA UDI | Class I | Active |
| NAR Kit | 85-2679 | FDA UDI | N/A | Active |
| NAR Kit | 85-0192 | FDA UDI | N/A | Active |
| Nar | 85-4840 | FDA UDI | Class I | Active |
| Nar | 85-1994 | FDA UDI | N/A | Active |
| Nar | 80-1664 | FDA UDI | Class I | Active |
| NAR Kit | 85-0013 | FDA UDI | N/A | Active |
| NAR Kit | 80-0416 | FDA UDI | N/A | Active |
| Nar | 85-1958-TLS | FDA UDI | Class I | Active |
| Nar | 85-4458 | FDA UDI | Class I | Active |
| Nar | 85-4709 | FDA UDI | Class I | Active |
| Nar | 85-4292 | FDA UDI | Class I | Active |
| Nar | 85-2347 | FDA UDI | Class I | Active |
| Nar | 80-1769 | FDA UDI | Class I | Active |
| Nar | 85-4109 | FDA UDI | N/A | Active |
| Nar | 85-4016 | FDA UDI | N/A | Active |
| Nar | 85-4456 | FDA UDI | Class I | Active |
| Nar | 85-3495 | FDA UDI | N/A | Active |
| NAR Kit | 85-0055 | FDA UDI | N/A | Active |
| Nar | 85-4774 | FDA UDI | Class I | Active |
| Nar | 85-4091 | FDA UDI | N/A | Active |
| Nar | 85-1187 | FDA UDI | N/A | Active |
| Nar | 85-3113 | FDA UDI | N/A | Active |
| Nar | 85-3356 | FDA UDI | N/A | Active |
| Nar | 85-4351 | FDA UDI | Class I | Active |
| Nar | 85-3288 | FDA UDI | N/A | Active |
| Nar | 85-4148 | FDA UDI | N/A | Active |
| Nar | 10-0063 | FDA UDI | Class I | Active |
| Nar | 80-1431 | FDA UDI | Class I | Active |
| Nar | 84-0104 | FDA UDI | N/A | Active |
| NAR Kit | 80-0187 | FDA UDI | N/A | Active |
| Nar | 85-3468 | FDA UDI | N/A | Active |
| Nar | 85-4202 | FDA UDI | N/A | Active |
| Nar | 85-2819 | FDA UDI | N/A | Active |
| Nar | 80-0975 | FDA UDI | N/A | Active |
| Nar | 85-4948 | FDA UDI | N | Active |
| Nar | 20-0017 | FDA UDI | Class I | Active |
| Nar | 85-4227 | FDA UDI | N/A | Active |
| Nar | 80-1098 | FDA UDI | N/A | Active |
| Nar | 85-3045 | FDA UDI | N/A | Active |
| Nar | 85-2571 | FDA UDI | N/A | Active |
| NAR Kit | 85-0667 | FDA UDI | N/A | Active |
| Nar | 82-0077 | FDA UDI | Class I | Active |
| Nar | 80-0453 | FDA UDI | N/A | Active |
| Nar | 85-2998 | FDA UDI | N/A | Active |
Related Companies
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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 |