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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 55 of 72

Device	Model / Reference	Registries	Class	Status
Nar	80-1697	FDA UDI	Class I	Active
NAR Kit	85-2488	FDA UDI	N/A	Active
NAR Kit	80-0001	FDA UDI	N/A	Active
Nar	85-1406	FDA UDI	N/A	Active
Nar	85-1217	FDA UDI	N/A	Active
Nar	80-1499	FDA UDI	N/A	Active
NAR Kit	85-1946	FDA UDI	N/A	Active
Nar	84-0157	FDA UDI	Class I	Active
Nar	85-4830	FDA UDI	Class I	Active
NAR Kit	85-3201	FDA UDI	N/A	Active
Nar	85-1258	FDA UDI	N/A	Active
Nar	85-4897	FDA UDI	Class I	Active
Nar	85-4324	FDA UDI	N	Active
Nar	30-0012	FDA UDI	Class I	Active
Nar	85-3995	FDA UDI	Class I	Active
Nar	85-4158	FDA UDI	N/A	Active
Nar	85-3198	FDA UDI	N/A	Active
NAR Kit	85-2697	FDA UDI	N/A	Active
Nar	20-0001	FDA UDI	Class I	Active
Nar	85-2207	FDA UDI	N/A	Active
Nar	85-4373	FDA UDI	Class I	Active
NAR Kit	85-1792	FDA UDI	N/A	Active
NAR Kit	85-0005	FDA UDI	N/A	Active
Nar	80-1425	FDA UDI	Class I	Active
Nar	80-1051	FDA UDI	N/A	Active
NAR Kit	80-0574	FDA UDI	N/A	Active
Nar	85-1814	FDA UDI	N/A	Active
NAR Kit	85-2898	FDA UDI	N/A	Active
Nar	85-4738	FDA UDI	Class I	Active
Nar	85-4865	FDA UDI	Class I	Active
Nar	80-1466	FDA UDI	Class I	Active
Nar	85-4279	FDA UDI	N/A	Active
Nar	85-4414	FDA UDI	Class I	Active
Nar	85-3833	FDA UDI	N/A	Active
Nar	85-3279	FDA UDI	N/A	Active
Nar	80-1822	FDA UDI	N	Active
Nar	80-1687	FDA UDI	Class I	Active
NAR Kit	ZZ-0388	FDA UDI	N/A	Active
Nar	85-4816	FDA UDI	Class I	Active
Nar	85-3315	FDA UDI	N/A	Active
Nar	85-3227	FDA UDI	N/A	Active
Nar	85-1841	FDA UDI	N/A	Active
NAR Kit	85-2834	FDA UDI	N/A	Active
Nar	85-4782	FDA UDI	Class I	Active
Nar	85-4145	FDA UDI	N/A	Active
Nar	85-4098	FDA UDI	N/A	Active
NAR Kit	80-1209	FDA UDI	N/A	Active
Nar	85-3997	FDA UDI	N/A	Active
Nar	85-3866	FDA UDI	N/A	Active
Nar	85-3816	FDA UDI	N/A	Active

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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