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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 70 of 72

Device	Model / Reference	Registries	Class	Status
NAR Kit	85-0009	FDA UDI	N/A	Active
Nar	85-4507	FDA UDI	Class I	Active
Nar	80-1142	FDA UDI	N/A	Active
Nar	85-2370	FDA UDI	N/A	Active
Nar	85-2500	FDA UDI	N/A	Active
NAR Kit	85-3415	FDA UDI	N/A	Active
NAR Kit	85-3343	FDA UDI	N/A	Active
NAR Kit	80-0874	FDA UDI	N/A	Active
NAR Kit	85-2050	FDA UDI	N/A	Active
NAR Kit	80-1026	FDA UDI	N/A	Active
NAR Kit	84-0023	FDA UDI	N/A	Active
NAR Kit	85-1488	FDA UDI	N/A	Active
NAR Kit	85-2997	FDA UDI	N/A	Active
NAR Kit	80-0014	FDA UDI	N/A	Active
NAR Kit	85-0017	FDA UDI	N/A	Active
NAR Kit	85-0189	FDA UDI	N/A	Active
NAR Kit	85-2532	FDA UDI	N/A	Active
NAR Kit	85-1403	FDA UDI	N/A	Active
NAR Kit	80-0407	FDA UDI	N/A	Active
NAR Kit	85-2891	FDA UDI	N/A	Active
NAR Kit	80-0488	FDA UDI	Class I	Active
NAR Kit	85-0518	FDA UDI	N/A	Active
NAR Kit	80-0168	FDA UDI	N/A	Active
NAR Kit	80-0410	FDA UDI	N/A	Unknown
NAR Kit	80-0158	FDA UDI	N/A	Active
NAR Kit	85-1551	FDA UDI	N/A	Active
Black Talon	ZZ-0277	FDA UDI	Class I	Active
NAR Kit	85-1420	FDA UDI	N/A	Active
NAR Kit	85-0791	FDA UDI	N/A	Active
NAR Kit	85-3216	FDA UDI	N/A	Active
NAR Kit	85-0775	FDA UDI	N/A	Active
NAR Tracheostomy Kit	10-0048	FDA UDI	N/A	Unknown
NAR Kit	85-3146	FDA UDI	N/A	Active
NAR Kit	85-2746	FDA UDI	N/A	Active
NAR Kit	85-1429	FDA UDI	N/A	Active
NAR Kit	85-2644	FDA UDI	N/A	Active
NAR Kit	85-1504	FDA UDI	N/A	Unknown
NAR Kit	85-0049	FDA UDI	N/A	Active
NAR Kit	80-0444	FDA UDI	N/A	Active
NAR Kit	85-3510	FDA UDI	N/A	Active
NAR Kit	80-0983	FDA UDI	N/A	Active
NAR Kit	85-1555	FDA UDI	N/A	Unknown
NAR Kit	80-0136	FDA UDI	N/A	Unknown
NAR Kit	80-0181	FDA UDI	Class I	Active
NAR Kit	10-0053	FDA UDI	N/A	Active
NAR Kit	85-1305	FDA UDI	N/A	Active
NAR Kit	85-3636	FDA UDI	N/A	Active
NAR Kit	85-2985	FDA UDI	N/A	Active
NAR Kit	82-0052	FDA UDI	N/A	Active
NAR Kit	85-1241	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