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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 9 of 72

Device	Model / Reference	Registries	Class	Status
NAR Kit	85-1424	FDA UDI	N/A	Active
NAR Kit	85-1425	FDA UDI	N/A	Active
Nar	85-3366	FDA UDI	N/A	Active
Nar	84-0151	FDA UDI	Class I	Active
NAR Kit	85-3266	FDA UDI	N/A	Active
Nar	85-3153	FDA UDI	N/A	Active
Nar	85-1862	FDA UDI	N/A	Active
Nar	85-4582	FDA UDI	Class I	Active
Nar	85-1710	FDA UDI	N/A	Active
NAR Kit	85-2315	FDA UDI	N/A	Active
NAR Kit	85-1363	FDA UDI	N/A	Unknown
NAR Kit	84-0074	FDA UDI	N/A	Active
NAR Kit	80-0159O	FDA UDI	N/A	Unknown
Nar	80-0924	FDA UDI	Class I	Active
Nar	85-4772	FDA UDI	Class I	Active
NAR Kit	85-2555	FDA UDI	N/A	Active
Nar	85-3848	FDA UDI	N/A	Active
Nar	85-4328	FDA UDI	Class II	Active
Nar	85-3847	FDA UDI	N/A	Active
Nar	85-1961	FDA UDI	N/A	Active
Nar	85-4190	FDA UDI	N/A	Active
Nar	85-4868	FDA UDI	Class I	Active
NAR Kit	85-1596	FDA UDI	N/A	Active
NAR Kit	85-3179	FDA UDI	N/A	Active
Nar	85-4404	FDA UDI	Class I	Active
Nar	84-0126	FDA UDI	N/A	Active
Nar	85-4239	FDA UDI	N/A	Active
NAR Kit	83-0025	FDA UDI	N/A	Active
Nar	80-0880	FDA UDI	N/A	Active
NAR Kit	85-3281	FDA UDI	N/A	Active
NAR Kit	85-0915	FDA UDI	N/A	Active
Nar	85-4732	FDA UDI	Class I	Active
NAR Kit	80-0515	FDA UDI	N/A	Active
NAR Kit	85-0936	FDA UDI	N/A	Active
Nar	85-3708	FDA UDI	N/A	Active
NAR Kit	ZZ-0777	FDA UDI	N/A	Active
NAR Kit	85-1464	FDA UDI	N/A	Active
Nar	85-4020	FDA UDI	N/A	Active
NAR Kit	80-0979	FDA UDI	N/A	Active
Nar	85-1442	FDA UDI	N/A	Active
Nar	85-1902	FDA UDI	Class I	Active
Nar	85-4702	FDA UDI	Class I	Active
Nar	80-1083	FDA UDI	N/A	Active
Nar	88-0001	FDA UDI	Class I	Active
Nar	85-3242	FDA UDI	N/A	Active
NAR Kit	85-3253	FDA UDI	N/A	Active
Nar	85-2332	FDA UDI	N/A	Active
Nar	85-3490	FDA UDI	N/A	Active
Nar	85-2824	FDA UDI	N/A	Active
Nar	80-1559	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