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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 22 of 72

Device	Model / Reference	Registries	Class	Status
NAR Kit	80-0917	FDA UDI	N/A	Unknown
Nar	85-1543	FDA UDI	N/A	Active
Nar	85-1633	FDA UDI	N/A	Active
NAR Kit	85-2002	FDA UDI	N/A	Active
NAR Kit	85-1327	FDA UDI	N/A	Active
NAR Kit	85-0198	FDA UDI	N/A	Unknown
Nar	85-3390	FDA UDI	N/A	Active
NAR Kit	80-0947	FDA UDI	N/A	Active
Nar	85-2515	FDA UDI	N/A	Active
Nar	85-4211	FDA UDI	Class I	Active
Nar	85-4922	FDA UDI	Class I	Active
NAR Kit	80-0427	FDA UDI	N/A	Active
NAR Kit	85-0184	FDA UDI	N/A	Unknown
NAR Kit	85-0834	FDA UDI	N/A	Active
Nar	85-2383	FDA UDI	N/A	Active
NAR Kit	85-2199	FDA UDI	N/A	Active
Nar	90-0108	FDA UDI	Class I	Active
NAR Kit	85-1006	FDA UDI	N/A	Unknown
NAR Kit	85-2220	FDA UDI	N/A	Active
Nar	85-4136	FDA UDI	Class I	Active
Nar	85-4564	FDA UDI	Class I	Active
Nar	85-4111	FDA UDI	N/A	Active
Nar	85-4864	FDA UDI	Class I	Active
Nar	85-3213	FDA UDI	N/A	Active
NAR Kit	85-1864	FDA UDI	N/A	Active
Tracheal Tube	ZZ-0269	FDA UDI	Class II	Unknown
Nar	85-2531	FDA UDI	N/A	Active
Nar	85-3442	FDA UDI	N/A	Active
Nar	85-1880	FDA UDI	N/A	Active
NAR Kit	85-1991	FDA UDI	N/A	Active
NAR Kit	85-1421	FDA UDI	N/A	Active
Nar	85-3722	FDA UDI	N/A	Active
Nar	85-4836	FDA UDI	N	Active
Nar	85-4330	FDA UDI	Class I	Active
Nar	85-3966	FDA UDI	N/A	Active
Nar	85-2239	FDA UDI	N/A	Active
NAR Kit	85-2645	FDA UDI	N/A	Active
Nar	85-3099	FDA UDI	N/A	Active
NAR Kit	85-2936	FDA UDI	N/A	Active
Nar	88-0021	FDA UDI	Class I	Active
NAR Kit	85-3183	FDA UDI	N/A	Unknown
Nar	85-4890	FDA UDI	Class I	Active
Nar	85-4039	FDA UDI	N/A	Active
Nar	85-1524	FDA UDI	N/A	Active
NAR Kit	85-1776	FDA UDI	N/A	Active
Nar	85-4088	FDA UDI	N/A	Active
NAR Kit	85-2469	FDA UDI	N/A	Active
Nar	85-4560	FDA UDI	Class I	Active
NAR Kit	80-0505	FDA UDI	N/A	Active
NAR Kit	85-3501	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