Is this your brand? Sign in to claim ownership.
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 4 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NAR Kit | 85-3039 | FDA UDI | N/A | Active |
| NAR Kit | 20-0002 | FDA UDI | Class I | Active |
| Nar | 88-0004 | FDA UDI | Class I | Active |
| NAR Kit | 85-2800 | FDA UDI | Class I | Active |
| Nar | 77-0074 | FDA UDI | Class I | Active |
| Nar | 85-1340 | FDA UDI | N/A | Active |
| NAR Kit | 85-2830 | FDA UDI | N/A | Active |
| NAR Kit | 80-1093 | FDA UDI | N/A | Active |
| Nar | 85-4535 | FDA UDI | Class I | Active |
| Nar | 85-3817 | FDA UDI | N/A | Active |
| Nar | 85-0715 | FDA UDI | N/A | Active |
| Nar | 85-4411 | FDA UDI | Class I | Active |
| Nar | 85-4036 | FDA UDI | N/A | Active |
| Nar | 85-3038 | FDA UDI | N/A | Active |
| Nar | 80-0861 | FDA UDI | N/A | Active |
| NAR Tracheal Hook | 10-0020 | FDA UDI | Class I | Active |
| NAR Kit | 80-0070 | FDA UDI | N/A | Active |
| Nar | 85-1064 | FDA UDI | N/A | Active |
| Nar | 85-3303 | FDA UDI | N/A | Active |
| Nar | 84-0105 | FDA UDI | N/A | Active |
| Nar | 85-4884 | FDA UDI | Class I | Active |
| NAR Kit | 85-2352 | FDA UDI | N/A | Active |
| NAR Kit | 80-0981 | FDA UDI | N/A | Active |
| Nar | 85-4531 | FDA UDI | Class I | Active |
| Nar | 85-3524 | FDA UDI | N/A | Active |
| Nar | 85-2599 | FDA UDI | N/A | Active |
| Nar | 85-2901 | FDA UDI | N/A | Active |
| Nar | 85-1332 | FDA UDI | N/A | Active |
| NAR Kit | 84-0010 | FDA UDI | N/A | Active |
| Nar | 85-4275 | FDA UDI | Class I | Active |
| NAR Kit | 85-2159 | FDA UDI | N/A | Active |
| Nar | 85-4896 | FDA UDI | Class I | Active |
| Nar | 85-2072 | FDA UDI | N/A | Active |
| Nar | 85-1759 | FDA UDI | N/A | Active |
| Nar | 80-1420 | FDA UDI | N/A | Active |
| Nar | 85-3106 | FDA UDI | N/A | Active |
| Nar | 80-0133-TLS | FDA UDI | Class I | Active |
| Nar | 85-4561 | FDA UDI | Class I | Active |
| NAR Kit | 85-3550 | FDA UDI | N/A | Active |
| Nar | 85-3712 | FDA UDI | N/A | Active |
| NAR Kit | 85-1958 | FDA UDI | N/A | Active |
| Nar | 85-4501 | FDA UDI | Class II | Active |
| NAR Kit | 80-0212 | FDA UDI | N/A | Active |
| Nar | 85-4525 | FDA UDI | Class I | Active |
| Nar | 88-0003 | FDA UDI | Class I | Active |
| Nar | 85-3836 | FDA UDI | N/A | Active |
| NAR Kit | 80-1220 | FDA UDI | N/A | Active |
| NAR Kit | 80-0184 | FDA UDI | N/A | Unknown |
| Nar | 85-1418 | FDA UDI | N/A | Active |
| Nar | 85-1502 | FDA UDI | N/A | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
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 |