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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 8 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-4206	FDA UDI	N/A	Active
NAR Kit	85-3136	FDA UDI	N/A	Active
Nar	80-1561	FDA UDI	Class I	Active
NAR Kit	85-3508	FDA UDI	N/A	Active
Nar	80-1447	FDA UDI	N/A	Active
Nar	85-3612	FDA UDI	N/A	Active
Nar	85-3441	FDA UDI	N/A	Active
NAR Kit	85-2692	FDA UDI	N/A	Active
NAR Kit	85-0004	FDA UDI	N/A	Active
Junctional Emergency Treatment Tool (jett®)	30-0088	FDA UDI	Class II	Active
Nar	85-4180	FDA UDI	N/A	Active
Nar	ZZ-0298	FDA UDI	Class I	Active
NAR Kit	85-3436	FDA UDI	N/A	Active
NAR kit	80-1216	FDA UDI	N/A	Active
NAR Kit	80-0519	FDA UDI	N/A	Active
Nar	85-4069	FDA UDI	N/A	Active
Nar	85-3799	FDA UDI	N/A	Active
Nar	85-4742	FDA UDI	N	Active
Nar	85-2637	FDA UDI	N/A	Active
NAR Kit	80-1150	FDA UDI	N/A	Active
NAR Kit	85-2609	FDA UDI	N/A	Active
Nar	80-0862	FDA UDI	N/A	Active
Nar	85-4274	FDA UDI	Class I	Active
Nar	85-4673	FDA UDI	Class I	Active
Nar	85-3632	FDA UDI	N/A	Active
Nar	85-0411	FDA UDI	N/A	Active
NAR Kit	10-0019	FDA UDI	N/A	Unknown
Nar	85-2569	FDA UDI	N/A	Active
Nar	85-4526	FDA UDI	Class I	Active
Nar	80-1168	FDA UDI	N/A	Active
NAR Kit	85-1387	FDA UDI	N/A	Active
NAR Kit	80-0420	FDA UDI	N/A	Active
NAR Kit	80-1048	FDA UDI	N/A	Active
Nar	80-1568	FDA UDI	N/A	Active
Nar	85-4694	FDA UDI	N	Active
Nar	85-3709	FDA UDI	N/A	Active
Nar	85-2070-TLS	FDA UDI	Class I	Active
Black Talon	ZZ-0215	FDA UDI	Class I	Active
Nar	85-4660	FDA UDI	Class I	Active
Nar	80-0584	FDA UDI	N/A	Active
NAR Kit	85-0183	FDA UDI	N/A	Unknown
Nar	85-4874	FDA UDI	Class I	Active
Nar	80-1580	FDA UDI	Class I	Active
Nar	80-1172	FDA UDI	N/A	Active
Nar	85-2796	FDA UDI	N/A	Active
NAR Kit	85-1307	FDA UDI	N/A	Active
NAR Kit	84-0025	FDA UDI	N/A	Active
Nar	85-4950	FDA UDI	Class I	Active
NAR Kit	85-2519	FDA UDI	N/A	Active
Nar	85-4355	FDA UDI	N	Active

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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