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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 71 of 72

Device	Model / Reference	Registries	Class	Status
NAR Kit	85-1164	FDA UDI	N/A	Active
TACTICAL CricKIT	85-2798	FDA UDI	Class II	Active
NAR Kit	80-1213	FDA UDI	N/A	Active
NAR Kit	80-0426	FDA UDI	N/A	Active
NAR kit	84-0070	FDA UDI	N/A	Active
NAR Kit	80-0096	FDA UDI	N/A	Unknown
NAR Kit	85-2876	FDA UDI	N/A	Active
NAR Kit	85-1234	FDA UDI	N/A	Active
NAR Kit	85-3668	FDA UDI	N/A	Active
NAR Kit	85-3264	FDA UDI	N/A	Active
NAR Kit	85-2344	FDA UDI	N/A	Unknown
NAR Kit	85-3482	FDA UDI	N/A	Active
NAR Kit	70-0197	FDA UDI	N/A	Active
NAR Kit	80-0419	FDA UDI	N/A	Active
NAR Kit	85-3252	FDA UDI	N/A	Active
NAR Kit	85-2660	FDA UDI	N/A	Active
NAR Kit	85-0770	FDA UDI	N/A	Active
NAR Kit	80-0385	FDA UDI	N/A	Unknown
NAR Kit	85-1447	FDA UDI	N/A	Active
NAR Kit	85-3809	FDA UDI	N/A	Active
NAR Kit	85-2044	FDA UDI	N/A	Active
NAR Kit	85-3509	FDA UDI	N/A	Active
NAR Kit	85-1437	FDA UDI	N/A	Active
NAR Kit	85-2196	FDA UDI	N/A	Active
NAR Kit	80-0582	FDA UDI	N/A	Active
NAR Kit	85-1744	FDA UDI	N/A	Active
NAR Kit	85-3267	FDA UDI	N/A	Active
NAR Kit	80-0992	FDA UDI	N/A	Active
NAR Kit	80-0502	FDA UDI	N/A	Active
NAR Kit	80-0015	FDA UDI	N/A	Active
NAR Kit	85-1338	FDA UDI	N/A	Active
NAR Kit	85-3231	FDA UDI	N/A	Active
NAR Kit	82-0055	FDA UDI	N/A	Active
NAR Kit	85-3311	FDA UDI	N/A	Active
NAR Kit	80-0297	FDA UDI	N/A	Unknown
NAR Kit	85-0011	FDA UDI	N/A	Unknown
NAR Kit	80-0151	FDA UDI	N/A	Active
NAR Kit	85-2248	FDA UDI	N/A	Active
NAR Kit	85-1796	FDA UDI	N/A	Active
NAR Kit	85-1279	FDA UDI	N/A	Active
NAR Kit	85-1395	FDA UDI	N/A	Active
NAR Kit	85-3224	FDA UDI	N/A	Active
NAR Kit	85-2874	FDA UDI	N/A	Active
TACTICAL CricKIT	85-2524	FDA UDI	Class II	Active
NAR Kit	85-3702	FDA UDI	N/A	Active
NAR Kit	85-2704	FDA UDI	N/A	Active
NAR Kit	85-2533	FDA UDI	N/A	Active
NAR Kit	85-0998	FDA UDI	N/A	Active
NAR Kit	85-2713	FDA UDI	N/A	Active
NAR Kit	85-3247	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