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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 33 of 72

Device	Model / Reference	Registries	Class	Status
Nar	84-0149	FDA UDI	Class I	Active
Nar	77-0079	FDA UDI	Class I	Active
NAR Kit	85-0421	FDA UDI	N/A	Active
NAR Kit	80-0182	FDA UDI	N/A	Active
Nar	85-4409	FDA UDI	Class I	Active
Nar	84-0145	FDA UDI	Class I	Active
Nar	80-1574	FDA UDI	N/A	Active
Nar	80-1553	FDA UDI	Class I	Active
Nar	80-1730	FDA UDI	Class I	Active
Nar	85-2907	FDA UDI	N/A	Active
Nar	85-0970	FDA UDI	N/A	Active
Nar	80-1577	FDA UDI	Class I	Active
NAR Kit	84-0019	FDA UDI	N/A	Active
Nar	85-3571	FDA UDI	N/A	Active
Nar	85-1999	FDA UDI	N/A	Active
Nar	85-0956	FDA UDI	N/A	Active
Nar	80-0465	FDA UDI	N/A	Active
Nar	85-4410	FDA UDI	Class I	Active
Nar	85-3523	FDA UDI	N/A	Active
Nar	85-2280	FDA UDI	N/A	Active
NAR Kit	85-1317	FDA UDI	N/A	Active
Nar	85-3121	FDA UDI	N/A	Active
NAR Kit	82-0001	FDA UDI	N/A	Active
Nar	80-0864	FDA UDI	N/A	Active
Nar	85-2952	FDA UDI	N/A	Active
Nar	85-1914	FDA UDI	N/A	Active
Nar	85-2543	FDA UDI	N/A	Active
NAR Kit	80-0244	FDA UDI	N/A	Active
Nar	80-1132	FDA UDI	N/A	Active
NAR Kit	82-0028	FDA UDI	N/A	Active
Nar	80-1100	FDA UDI	N/A	Active
Life Warmer Quantum Blood and Fluid Warming System (IV Fluid ONLY Configuration)	63-5906	FDA UDI	Class II	Active
NAR Kit	85-2045	FDA UDI	N/A	Active
Nar	85-3349	FDA UDI	N/A	Active
Nar	85-4267	FDA UDI	Class II	Active
Nar	85-4572	FDA UDI	Class I	Active
Nar	85-3793	FDA UDI	N/A	Active
Nar	82-0044	FDA UDI	N/A	Active
NAR Kit	85-1738	FDA UDI	N/A	Active
Nar	85-4675	FDA UDI	Class I	Active
Nar	85-3760	FDA UDI	N/A	Active
NAR Kit	85-2354	FDA UDI	N/A	Active
NAR Kit	85-1950	FDA UDI	N/A	Active
Nar	85-3556	FDA UDI	N/A	Active
Nar	85-4670	FDA UDI	Class I	Active
Nar	85-3255	FDA UDI	N/A	Active
Nar	80-0015-TLS	FDA UDI	Class I	Active
Nar	85-3537	FDA UDI	N/A	Active
Nar	85-4407	FDA UDI	Class I	Active
Nar	85-3605	FDA UDI	N/A	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