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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 59 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-1943 | FDA UDI | N/A | Active |
| Nar | 85-4425 | FDA UDI | Class I | Active |
| Nar | 85-1583 | FDA UDI | N/A | Active |
| Nar | 85-4466 | FDA UDI | Class I | Active |
| Nar | 85-4759 | FDA UDI | Class I | Active |
| Nar | 85-3715 | FDA UDI | N/A | Active |
| NAR Kit | 85-1031 | FDA UDI | N/A | Active |
| Nar | 85-2409 | FDA UDI | N/A | Active |
| Nar | 85-4280 | FDA UDI | Class I | Active |
| NAR Kit | 85-2042 | FDA UDI | N/A | Active |
| Nar | 85-3504 | FDA UDI | N/A | Active |
| Nar | 85-1536 | FDA UDI | N/A | Active |
| Nar | 85-4314 | FDA UDI | Class I | Active |
| Nar | 85-1655 | FDA UDI | N/A | Active |
| NAR Kit | 85-0188 | FDA UDI | N/A | Unknown |
| Nar | 85-1905 | FDA UDI | N/A | Active |
| NAR Kit | 80-0447 | FDA UDI | N/A | Active |
| NAR Kit | 85-2940 | FDA UDI | N/A | Active |
| Nar | 85-1793 | FDA UDI | N/A | Active |
| NAR Kit | 85-3666 | FDA UDI | N/A | Active |
| NAR Kit | 84-0020 | FDA UDI | N/A | Active |
| NAR Kit | 85-2886 | FDA UDI | N/A | Active |
| NAR Kit | 80-0089 | FDA UDI | N/A | Active |
| NAR Kit | 85-1368 | FDA UDI | N/A | Active |
| NAR Kit | 85-1960 | FDA UDI | N/A | Active |
| NAR Kit | 70-0205 | FDA UDI | N/A | Active |
| Nar | 85-3270 | FDA UDI | N/A | Active |
| NAR Kit | 85-3644 | FDA UDI | N/A | Active |
| Nar | 85-2821 | FDA UDI | N/A | Active |
| NAR Kit | 85-1206 | FDA UDI | N/A | Active |
| Nar | 85-3352 | FDA UDI | N/A | Active |
| Nar | 80-1181 | FDA UDI | N/A | Active |
| Nar | 85-3930 | FDA UDI | N/A | Active |
| NAR Kit | 85-0187 | FDA UDI | N/A | Unknown |
| Nar | 80-1680 | FDA UDI | Class I | Active |
| Nar | 82-0048 | FDA UDI | N/A | Active |
| Nar | 85-1595 | FDA UDI | N/A | Active |
| Nar | 30-0182B | FDA UDI | Class I | Active |
| Nar | 85-4226 | FDA UDI | N/A | Active |
| Nar | 85-3923 | FDA UDI | N/A | Active |
| NAR Kit | 85-2151 | FDA UDI | N/A | Active |
| Nar | 85-1729 | FDA UDI | N/A | Active |
| Nar | 85-4939 | FDA UDI | Class I | Active |
| Nar | 85-4681 | FDA UDI | Class I | Active |
| Nar | 85-3962 | FDA UDI | N/A | Active |
| NAR Kit | 80-0985 | FDA UDI | N/A | Active |
| Nar | 85-1901 | FDA UDI | Class I | Active |
| Nar | 85-3263 | FDA UDI | N/A | Active |
| Nar | 85-1771 | FDA UDI | N/A | Active |
| Nar | 85-3700 | FDA UDI | N/A | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
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 |