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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 21 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-2520 | FDA UDI | N/A | Active |
| Nar | 85-4894 | FDA UDI | Class I | Active |
| Nar | 80-0913 | FDA UDI | N/A | Active |
| NAR Kit | 80-1210 | FDA UDI | N/A | Active |
| Nar | 85-2994 | FDA UDI | N/A | Active |
| Nar | 85-2046 | FDA UDI | N/A | Active |
| NAR Kit | 80-0892 | FDA UDI | N/A | Active |
| Nar | 85-3561 | FDA UDI | N/A | Active |
| NAR Kit | 80-1208 | FDA UDI | N/A | Active |
| NAR Kit | 85-0606 | FDA UDI | N/A | Active |
| Nar | 85-4419 | FDA UDI | Class I | Active |
| Nar | 80-1693 | FDA UDI | Class I | Active |
| Nar | 85-0940 | FDA UDI | N/A | Active |
| Nar | 85-4130 | FDA UDI | N/A | Active |
| NAR Kit | 85-3110 | FDA UDI | N/A | Active |
| Nar | 85-3650 | FDA UDI | N/A | Active |
| Nar | 85-4583 | FDA UDI | N | Active |
| Nar | 84-0071 | FDA UDI | N/A | Active |
| Nar | 85-2964 | FDA UDI | N/A | Active |
| Nar | 84-0011 | FDA UDI | N/A | Active |
| Nar | 85-3549 | FDA UDI | N/A | Active |
| Nar | 85-4376 | FDA UDI | N | Active |
| Nar | 85-3434 | FDA UDI | Class I | Active |
| NAR Kit | 85-1768 | FDA UDI | N/A | Active |
| Nar | 85-4655 | FDA UDI | Class I | Active |
| NAR Kit | 80-0087 | FDA UDI | N/A | Active |
| Nar | 85-1826 | FDA UDI | N/A | Active |
| Nar | 85-4232 | FDA UDI | N/A | Active |
| Nar | 85-2771 | FDA UDI | N/A | Active |
| NAR Kit | 85-1431 | FDA UDI | N/A | Unknown |
| Nar | 80-1653 | FDA UDI | Class I | Active |
| NAR Kit | 85-1764 | FDA UDI | N/A | Active |
| Nar | 80-1616 | FDA UDI | N | Active |
| Nar | 84-0156 | FDA UDI | Class I | Active |
| Nar | 85-4693 | FDA UDI | Class I | Active |
| Nar | 85-4086 | FDA UDI | N/A | Active |
| Nar | 84-0072 | FDA UDI | N/A | Active |
| NAR Kit | 80-0058 | FDA UDI | N/A | Unknown |
| Nar | 85-4508 | FDA UDI | Class I | Active |
| Nar | 85-1797 | FDA UDI | N/A | Active |
| NAR Kit | 85-3705 | FDA UDI | N/A | Active |
| Nar | 85-3619 | FDA UDI | N/A | Active |
| Nar | 82-0046 | FDA UDI | N/A | Active |
| Nar | 85-3993 | FDA UDI | Class I | Active |
| NAR Kit | 85-2037 | FDA UDI | N/A | Active |
| NAR Kit | 80-0211 | FDA UDI | N/A | Unknown |
| Nar | 85-2889 | FDA UDI | N/A | Active |
| Nar | 80-1688 | FDA UDI | Class I | Active |
| NAR Kit | 80-1046 | FDA UDI | N/A | Active |
| Nar | 85-3752 | 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 |