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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 24 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 85-0835 | FDA UDI | N/A | Active |
| Nar | 77-0076 | FDA UDI | Class I | Active |
| Nar | 80-1740 | FDA UDI | Class I | Active |
| Nar | 80-1717 | FDA UDI | Class I | Active |
| Nar | 85-2967 | FDA UDI | N/A | Active |
| NAR Kit | 85-1016 | FDA UDI | N/A | Active |
| Nar | 85-4555 | FDA UDI | Class I | Active |
| NAR Kit | 80-0118 | FDA UDI | N/A | Active |
| Nar | 85-3649 | FDA UDI | N/A | Active |
| Nar | 80-1055 | FDA UDI | N/A | Active |
| Nar | 84-0030 | FDA UDI | N/A | Active |
| Nar | 85-3554 | FDA UDI | N/A | Active |
| Nar | 85-3506 | FDA UDI | N/A | Active |
| Nar | 85-4923 | FDA UDI | Class I | Active |
| Nar | 80-1139 | FDA UDI | N/A | Active |
| Nar | 85-4674 | FDA UDI | Class I | Active |
| Nar | 85-4779 | FDA UDI | Class II | Active |
| Nar | 85-2578 | FDA UDI | N/A | Active |
| Nar | 84-0150 | FDA UDI | Class I | Active |
| NAR Kit | 10-0002 | FDA UDI | Class I | Active |
| Nar | 85-4081 | FDA UDI | N/A | Active |
| NAR Kit | 84-0031 | FDA UDI | N/A | Active |
| Nar | 70-0426 | FDA UDI | Class I | Active |
| Nar | 77-0093 | FDA UDI | Class I | Active |
| Nar | 80-1690 | FDA UDI | Class I | Active |
| Nar | 85-4646 | FDA UDI | Class I | Active |
| Nar | 85-1335 | FDA UDI | N/A | Active |
| Nar | 85-1944 | FDA UDI | N/A | Active |
| NAR Kit | 80-1058 | FDA UDI | N/A | Active |
| NAR Kit | 80-1004 | FDA UDI | N/A | Active |
| NAR Kit | 85-1281 | FDA UDI | N/A | Active |
| Nar | 85-4218 | FDA UDI | N/A | Unknown |
| Nar | 85-2537 | FDA UDI | N/A | Active |
| NAR Kit | 85-2481 | FDA UDI | N/A | Active |
| NAR Kit | 85-1886 | FDA UDI | N/A | Active |
| Nar | 85-3774 | FDA UDI | N/A | Active |
| NAR Kit | 85-1404 | FDA UDI | N/A | Active |
| NAR Kit | 80-0448 | FDA UDI | N/A | Active |
| Nar | 85-1436 | FDA UDI | N/A | Active |
| NAR Kit | 85-3041 | FDA UDI | N/A | Active |
| Nar | 82-0084 | FDA UDI | N | Active |
| NAR Kit | 82-0036 | FDA UDI | N/A | Active |
| Nar | 80-1631 | FDA UDI | Class I | Active |
| Nar | 80-1478 | FDA UDI | N/A | Active |
| NAR Kit | 85-2221 | FDA UDI | N/A | Active |
| Nar | 85-3341 | FDA UDI | N/A | Active |
| Nar | 85-3736 | FDA UDI | N/A | Active |
| Nar | 85-3876 | FDA UDI | N/A | Active |
| Nar | 85-4752 | FDA UDI | Class I | Active |
| Nar | 80-1052 | 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 |