Is this your brand? Sign in to claim ownership.

NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Country: US
Address: 35 TEDWALL COURT, Greer, SC, 29650
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3005034064
DUNS Number: —

Catalogue (3581)

Page 53 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-4901	FDA UDI	Class I	Active
Nar	85-4778	FDA UDI	Class I	Active
NAR Kit	85-3350	FDA UDI	N/A	Active
Nar	30-0031	FDA UDI	Class I	Active
NAR Kit	85-2232	FDA UDI	Class II	Active
NAR Kit	85-2902	FDA UDI	N/A	Active
NAR Kit	85-0008	FDA UDI	N/A	Active
Nar	85-2058	FDA UDI	N/A	Active
Life Warmer Quantum Thermal Infusion Set (TIS)	63-5903	FDA UDI	Class II	Active
Nar	80-1849	FDA UDI	Class I	Active
Nar	84-0032	FDA UDI	N/A	Active
Nar	85-3371	FDA UDI	N/A	Active
Nar	85-1909	FDA UDI	N/A	Active
Nar	85-1336	FDA UDI	N/A	Active
NAR Kit	85-1362	FDA UDI	N/A	Unknown
Nar	85-2107	FDA UDI	N/A	Active
Nar	80-0141	FDA UDI	Class I	Active
Nar	85-4719	FDA UDI	Class I	Active
Nar	85-1201	FDA UDI	Class I	Active
Nar	80-1573	FDA UDI	N/A	Active
NAR Kit	85-3625	FDA UDI	N/A	Active
Nar	85-4359	FDA UDI	N	Active
Nar	85-1706	FDA UDI	N/A	Active
Nar	77-0083	FDA UDI	Class I	Active
Nar	85-3897	FDA UDI	N/A	Active
Nar	85-3192	FDA UDI	N/A	Active
NAR Kit	85-1965	FDA UDI	N/A	Unknown
NAR Kit	85-3492	FDA UDI	N/A	Active
Nar	77-0077	FDA UDI	Class I	Active
NAR Kit	85-1434	FDA UDI	N/A	Active
NAR Kit	85-1037	FDA UDI	N/A	Active
Nar	85-4215	FDA UDI	N/A	Active
NAR Kit	85-1760	FDA UDI	N/A	Unknown
NAR Kit	85-0200	FDA UDI	N/A	Unknown
Nar	85-2575	FDA UDI	N/A	Active
Nar	85-1629	FDA UDI	N/A	Active
NAR Kit	80-0386	FDA UDI	N/A	Unknown
Nar	85-4886	FDA UDI	Class I	Active
NAR Kit	85-2464	FDA UDI	N/A	Active
Nar	85-4606	FDA UDI	Class I	Active
Nar	85-1715	FDA UDI	N/A	Active
NAR Kit	85-3457	FDA UDI	N/A	Active
Nar	85-2665	FDA UDI	N/A	Active
Nar	85-1750	FDA UDI	N/A	Active
NAR Kit	84-0013	FDA UDI	N/A	Active
Nar	85-4574	FDA UDI	Class I	Active
Nar	85-3346	FDA UDI	N/A	Active
NAR Kit	85-2487	FDA UDI	N/A	Active
Nar	85-2916	FDA UDI	N/A	Active
Nar	84-0029	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