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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 68 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-4309	FDA UDI	Class I	Active
NAR Kit	85-3071	FDA UDI	N/A	Active
NAR Kit	85-2330	FDA UDI	N/A	Active
Nar	85-1917	FDA UDI	N/A	Active
Nar	84-0170	FDA UDI	Class I	Active
Nar	20-0022	FDA UDI	Class I	Active
Nar	83-0027	FDA UDI	Class I	Active
NAR Kit	85-2912	FDA UDI	N/A	Active
Nar	85-2823	FDA UDI	N/A	Active
NAR Kit	80-0970	FDA UDI	N/A	Active
NAR kit	84-0073	FDA UDI	N/A	Active
Nar	85-1007	FDA UDI	N/A	Active
NAR Kit	80-1189	FDA UDI	N/A	Active
NAR Kit	85-1361	FDA UDI	N/A	Unknown
Nar	82-0040	FDA UDI	N/A	Active
Nar	85-2254	FDA UDI	N/A	Active
Nar	85-3858	FDA UDI	N/A	Active
NAR Kit	80-0450	FDA UDI	N/A	Active
Nar	85-3888	FDA UDI	N/A	Active
Nar	85-3203	FDA UDI	N/A	Active
Nar	85-2246	FDA UDI	N/A	Active
Nar	85-1748	FDA UDI	N/A	Active
Nar	30-0172	FDA UDI	Class I	Active
Nar	85-2815	FDA UDI	N/A	Active
NAR Kit	80-0980	FDA UDI	N/A	Active
NAR Kit	85-1377	FDA UDI	N/A	Active
Nar	85-0163	FDA UDI	N/A	Active
NAR Kit	85-2166	FDA UDI	N/A	Active
Nar	77-0100	FDA UDI	Class I	Active
Nar	85-4196	FDA UDI	N/A	Active
Nar	80-1837	FDA UDI	N	Active
Nar	80-1576	FDA UDI	Class I	Active
Nar	85-4137	FDA UDI	Class II	Active
NAR Kit	85-2556	FDA UDI	N/A	Active
Nar	85-4940	FDA UDI	Class I	Active
Nar	85-3933	FDA UDI	N/A	Active
NAR Kit	85-1396	FDA UDI	N/A	Active
Nar	85-2274	FDA UDI	N/A	Active
NAR Kit	85-0814	FDA UDI	N/A	Active
NAR Kit	80-0514	FDA UDI	N/A	Active
Nar	84-0026	FDA UDI	N/A	Active
Nar	85-4468	FDA UDI	Class I	Active
Nar	85-3314	FDA UDI	N/A	Active
Nar	85-3118	FDA UDI	N/A	Active
Nar	85-3126	FDA UDI	N/A	Active
Nar	85-2407	FDA UDI	N/A	Active
Nar	85-2244	FDA UDI	N/A	Active
NAR Kit	85-3228	FDA UDI	N/A	Active
NAR Kit	85-1416	FDA UDI	N/A	Active
Nar	85-4357	FDA UDI	Class I	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