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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 17 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-1689	FDA UDI	N/A	Active
NAR Kit	80-0097	FDA UDI	N/A	Active
Nar	85-4454	FDA UDI	N	Active
NAR Kit	85-1265	FDA UDI	N/A	Active
Nar	85-2513	FDA UDI	N/A	Active
Nar	85-4534	FDA UDI	Class I	Active
NAR Kit	85-2825	FDA UDI	N/A	Active
NAR Kit	85-1173	FDA UDI	Class I	Active
Nar	82-0067	FDA UDI	N	Active
Nar	30-0032	FDA UDI	Class I	Active
Nar	85-4951	FDA UDI	Class I	Active
Nar	85-2525	FDA UDI	N/A	Active
NAR Kit	80-1095	FDA UDI	N/A	Active
Nar	85-3173	FDA UDI	N/A	Active
NAR Kit	85-1807	FDA UDI	N/A	Active
NAR Kit	85-3230	FDA UDI	N/A	Active
Nar	80-0901	FDA UDI	N/A	Active
NAR Kit	85-3717	FDA UDI	N/A	Active
NAR Kit	85-3305	FDA UDI	N/A	Active
Nar	82-0041	FDA UDI	N/A	Active
Nar	85-2434	FDA UDI	N/A	Active
Nar	85-1122	FDA UDI	N/A	Active
Nar	85-1572	FDA UDI	N/A	Active
NAR Kit	80-0476	FDA UDI	N/A	Active
NAR Kit	85-2040	FDA UDI	N/A	Active
Nar	85-3070	FDA UDI	N/A	Active
Nar	84-0033	FDA UDI	Class I	Active
Nar	85-4931	FDA UDI	Class I	Active
Nar	85-1765	FDA UDI	N/A	Active
NAR Kit	80-0982	FDA UDI	N/A	Active
Nar	85-1290	FDA UDI	N/A	Active
Nar	77-0086	FDA UDI	Class I	Active
Nar	10-0037	FDA UDI	Class I	Active
Nar	85-4295	FDA UDI	Class I	Active
Nar	84-0097	FDA UDI	N/A	Active
Nar	85-4642	FDA UDI	Class I	Active
Nar	85-4590	FDA UDI	Class I	Active
Black Talon	70-0001	FDA UDI	Class I	Active
Nar	85-4661	FDA UDI	N	Active
NAR Kit	80-0225	FDA UDI	N/A	Active
Nar	85-4243	FDA UDI	N/A	Active
NAR Kit	85-0692	FDA UDI	N/A	Active
Nar	85-3785	FDA UDI	N/A	Active
NAR kit	84-0012	FDA UDI	N/A	Active
Nar	80-1470	FDA UDI	Class I	Active
Nar	80-1801	FDA UDI	Class I	Active
Nar	85-2722	FDA UDI	N/A	Active
Nar	80-1670	FDA UDI	Class I	Active
Nar	85-2888	FDA UDI	N/A	Active
Nar	80-0883	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