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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 2 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-1581 | FDA UDI | Class I | Active |
| Nar | 30-0182 | FDA UDI | Class I | Active |
| Nar | 85-4089 | FDA UDI | N/A | Active |
| Nar | 80-1824 | FDA UDI | N | Active |
| Nar | 85-3430 | FDA UDI | Class I | Active |
| Nar | 80-1140 | FDA UDI | N/A | Active |
| Nar | 84-0018 | FDA UDI | N/A | Active |
| NAR Kit | 85-2061 | FDA UDI | N/A | Active |
| Nar | 85-3328 | FDA UDI | N/A | Active |
| Nar | 85-4142 | FDA UDI | N/A | Active |
| NAR Kit | 80-1141 | FDA UDI | N/A | Active |
| NAR Kit | 85-2708 | FDA UDI | N/A | Active |
| NAR Kit | 80-1028 | FDA UDI | N/A | Active |
| Nar | 80-0873 | FDA UDI | N/A | Active |
| Nar | 85-3579 | FDA UDI | N/A | Active |
| NAR Kit | 85-2614 | FDA UDI | N/A | Active |
| NAR Kit | 85-1627 | FDA UDI | N/A | Active |
| Nar | 80-1636 | FDA UDI | Class I | Active |
| Nar | 85-4055 | FDA UDI | N/A | Active |
| Nar | 85-3960 | FDA UDI | N/A | Active |
| NAR Kit | 85-1617 | FDA UDI | N/A | Active |
| Nar | 85-4105 | FDA UDI | N/A | Active |
| Nar | 85-1601 | FDA UDI | N/A | Active |
| Nar | 85-3322 | FDA UDI | N/A | Active |
| Nar | 80-1085 | FDA UDI | N/A | Active |
| Nar | 85-4616 | FDA UDI | Class I | Active |
| Nar | 80-1174 | FDA UDI | N/A | Active |
| NAR Kit | 85-1399 | FDA UDI | N/A | Active |
| Nar | 80-1762 | FDA UDI | Class I | Active |
| Nar | 85-4686 | FDA UDI | N | Active |
| Nar | 80-1770 | FDA UDI | Class I | Active |
| Nar | 85-1125 | FDA UDI | N/A | Active |
| Nar | 85-2433 | FDA UDI | N/A | Active |
| Nar | 85-3926 | FDA UDI | N/A | Active |
| Nar | 80-1050 | FDA UDI | N/A | Active |
| Nar | 85-3444 | FDA UDI | N/A | Active |
| Nar | 85-3493 | FDA UDI | N/A | Active |
| NAR Kit | 80-0470 | FDA UDI | N/A | Active |
| NAR Kit | 85-1767 | FDA UDI | N/A | Active |
| NAR Kit | 85-1342 | FDA UDI | N/A | Unknown |
| Nar | 30-0127 | FDA UDI | Class I | Active |
| NAR Kit | 85-3439 | FDA UDI | N/A | Active |
| Nar | 85-4076 | FDA UDI | N/A | Active |
| Nar | 80-1131 | FDA UDI | N/A | Active |
| Nar | 85-3193 | FDA UDI | N/A | Active |
| Nar | 85-2161 | FDA UDI | N/A | Active |
| NAR Kit | 85-3381 | FDA UDI | N/A | Active |
| Nar | 85-3164 | FDA UDI | N/A | Active |
| NAR Kit | 80-0922 | FDA UDI | N/A | Active |
| Nar | 85-3116 | FDA UDI | N/A | Active |
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 |