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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 16 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 82-0033 | FDA UDI | N/A | Active |
| Nar | 85-3093 | FDA UDI | N/A | Active |
| Nar | 80-1619 | FDA UDI | Class I | Active |
| Nar | 85-4402 | FDA UDI | Class I | Active |
| NAR Kit | 85-3801 | FDA UDI | N/A | Active |
| Nar | 80-1435 | FDA UDI | N/A | Active |
| Nar | 80-1130 | FDA UDI | N/A | Active |
| Nar | 85-2231 | FDA UDI | N/A | Active |
| Nar | 85-3924 | FDA UDI | N/A | Active |
| Nar | 85-3784 | FDA UDI | N/A | Active |
| NAR Kit | 85-2563 | FDA UDI | N/A | Active |
| Nar | 85-3052 | FDA UDI | N/A | Active |
| Nar | 85-2878 | FDA UDI | N/A | Active |
| Nar | 85-1604 | FDA UDI | N/A | Active |
| Nar | 85-3137 | FDA UDI | N/A | Active |
| Nar | 85-2991 | FDA UDI | N/A | Active |
| Nar | 83-0000 | FDA UDI | Class II | Active |
| Nar | 85-3323 | FDA UDI | N/A | Active |
| Nar | 85-3177 | FDA UDI | N/A | Active |
| Nar | 80-1682 | FDA UDI | Class I | Active |
| Nar | 85-4954 | FDA UDI | Class I | Active |
| Nar | 85-3530 | FDA UDI | N/A | Active |
| Nar | 85-3558 | FDA UDI | N/A | Active |
| Nar | 85-1894 | FDA UDI | N/A | Active |
| Nar | 80-1492 | FDA UDI | N/A | Active |
| Nar | 85-1414 | FDA UDI | N/A | Active |
| NAR Kit | 80-0968 | FDA UDI | N/A | Active |
| NAR Kit | 85-1550 | FDA UDI | N/A | Active |
| NAR Kit | 85-2297 | FDA UDI | N/A | Active |
| Nar | 80-0867 | FDA UDI | N/A | Active |
| Nar | 85-4251 | FDA UDI | Class I | Active |
| NAR Kit | 85-1215 | FDA UDI | N/A | Active |
| NAR Kit | 85-1278 | FDA UDI | N/A | Unknown |
| Nar Tactical Suction Device | 10-0018 | FDA UDI | Class I | Active |
| NAR Kit | 85-1341 | FDA UDI | N/A | Active |
| Nar | 80-0885 | FDA UDI | N/A | Active |
| Nar | 85-2666 | FDA UDI | N/A | Active |
| Nar | 80-0938 | FDA UDI | N/A | Active |
| NAR Kit | 85-2920 | FDA UDI | N/A | Active |
| Nar | 80-1579 | FDA UDI | Class I | Active |
| Nar | 85-2999 | FDA UDI | N/A | Active |
| Nar | 85-3674 | FDA UDI | N/A | Active |
| Nar | 85-2068 | FDA UDI | N/A | Active |
| NAR Kit | 85-1062 | FDA UDI | N/A | Active |
| NAR Kit | 80-0516 | FDA UDI | N/A | Unknown |
| NAR Kit | 85-0965 | FDA UDI | N/A | Active |
| Nar | 85-3925 | FDA UDI | N/A | Active |
| Nar | 85-1927 | FDA UDI | N/A | Active |
| Nar | 85-3261 | FDA UDI | N/A | Active |
| NAR Kit | 85-3713 | 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 |