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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 50 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-1803 | FDA UDI | Class I | Active |
| NAR Kit | 80-1038 | FDA UDI | N/A | Active |
| Nar | 85-3275 | FDA UDI | N/A | Active |
| Nar | 84-0094 | FDA UDI | N/A | Active |
| Nar | 85-3599 | FDA UDI | N/A | Active |
| NAR Kit | 80-0278 | FDA UDI | N/A | Unknown |
| NAR Kit | 85-3085 | FDA UDI | N/A | Active |
| NAR Kit | 85-0961 | FDA UDI | N/A | Active |
| Nar | 85-3654 | FDA UDI | N/A | Active |
| Nar | 84-0158 | FDA UDI | Class I | Active |
| NAR Kit | 85-3445 | FDA UDI | N/A | Active |
| Nar | 85-3432 | FDA UDI | Class I | Active |
| NAR Kit | 85-3333 | FDA UDI | N/A | Active |
| Nar | 80-0577 | FDA UDI | N/A | Active |
| NAR Kit | 80-0309 | FDA UDI | N/A | Active |
| NAR Kit | 80-0059 | FDA UDI | N/A | Active |
| Nar | 80-1825 | FDA UDI | N | Active |
| Nar | 85-1940 | FDA UDI | N/A | Active |
| Nar | 85-3953 | FDA UDI | N/A | Active |
| Nar | 82-0030 | FDA UDI | N/A | Active |
| Nar | 85-1851 | FDA UDI | N/A | Active |
| Nar | 85-4146 | FDA UDI | N/A | Active |
| Nar | 85-3256 | FDA UDI | N/A | Active |
| Nar | 80-0461 | FDA UDI | N/A | Active |
| Nar | 85-4895 | FDA UDI | Class I | Active |
| Nar | 84-0139 | FDA UDI | N/A | Active |
| Nar | 85-3531 | FDA UDI | N/A | Active |
| Nar | 85-4735 | FDA UDI | Class I | Active |
| Nar | 80-1628 | FDA UDI | Class I | Active |
| Nar | 85-3174 | FDA UDI | N/A | Active |
| Nar | 85-4852 | FDA UDI | Class I | Active |
| Nar | 85-3804 | FDA UDI | N/A | Active |
| NAR Kit | 85-0841 | FDA UDI | N/A | Active |
| Nar | 85-2943 | FDA UDI | N/A | Active |
| Nar | 85-2987 | FDA UDI | N/A | Active |
| NAR Kit | 85-0883 | FDA UDI | N/A | Active |
| NAR Kit | 85-0502 | FDA UDI | N/A | Active |
| NAR Kit | 85-0686 | FDA UDI | N/A | Active |
| Nar | 85-3172 | FDA UDI | N/A | Active |
| NAR Kit | 80-0318 | FDA UDI | N/A | Unknown |
| Nar | 85-2067 | FDA UDI | N/A | Active |
| Nar | 85-0924 | FDA UDI | Class I | Active |
| NAR Kit | 85-3084 | FDA UDI | N/A | Active |
| NAR Kit | 80-1067 | FDA UDI | N/A | Active |
| NAR Kit | 85-1568 | FDA UDI | N/A | Active |
| NAR Kit | 85-1405 | FDA UDI | N/A | Active |
| NAR Kit | 85-0934 | FDA UDI | N/A | Active |
| Nar | 85-2773 | FDA UDI | N/A | Active |
| NAR Kit | 85-1478 | FDA UDI | N/A | Active |
| Nar | 80-1678 | FDA UDI | Class I | 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 |