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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 65 of 72

Device	Model / Reference	Registries	Class	Status
NAR Kit	85-3382	FDA UDI	N/A	Active
NAR Kit	85-0631	FDA UDI	N/A	Active
Nar	80-1679	FDA UDI	Class I	Active
Nar	85-2875	FDA UDI	N/A	Active
Nar	80-0575	FDA UDI	N/A	Active
NAR Kit	85-1210	FDA UDI	N/A	Active
Nar	85-4481	FDA UDI	Class I	Active
Nar	85-4341	FDA UDI	Class I	Active
NAR Kit	85-2262	FDA UDI	N/A	Active
Nar	80-1555	FDA UDI	Class I	Active
Nar	85-4731	FDA UDI	Class I	Active
NAR Kit	85-2993	FDA UDI	N/A	Active
Nar	85-1561	FDA UDI	N/A	Active
Nar	85-3835	FDA UDI	N/A	Active
NAR Kit	82-0054	FDA UDI	N/A	Active
NAR Kit	80-0446	FDA UDI	N/A	Active
Nar	30-0071	FDA UDI	Class I	Active
NAR Kit	85-2635	FDA UDI	N/A	Active
Nar	88-0036	FDA UDI	Class I	Active
Nar	85-1656	FDA UDI	N/A	Active
Nar	85-2357	FDA UDI	N/A	Active
Nar	85-3211	FDA UDI	N/A	Active
Nar	85-4571	FDA UDI	Class I	Active
NAR Kit	80-1143	FDA UDI	N/A	Active
Nar	85-4710	FDA UDI	N	Active
Nar	85-1924	FDA UDI	N/A	Active
Nar	82-0060	FDA UDI	N/A	Active
TACTICAL CricKIT	85-3294	FDA UDI	Class II	Active
Nar	85-4290	FDA UDI	Class I	Active
Nar	10-0051	FDA UDI	Class I	Active
Nar	85-2626	FDA UDI	N/A	Active
Nar	85-1866	FDA UDI	N/A	Active
Nar	85-3766	FDA UDI	N/A	Active
NAR Kit	85-1650	FDA UDI	N/A	Active
Nar	77-0090	FDA UDI	Class I	Active
NAR Kit	85-1069	FDA UDI	N/A	Active
Nar	85-3906	FDA UDI	N/A	Active
Nar	80-1570	FDA UDI	N/A	Active
Nar	30-0291	FDA UDI	Class I	Active
Nar	85-3387	FDA UDI	N/A	Active
NAR Kit	85-0054	FDA UDI	N/A	Active
Nar	84-0155	FDA UDI	Class I	Active
Nar	80-1613	FDA UDI	N	Active
Nar	85-4375	FDA UDI	Class I	Active
Nar	85-4920	FDA UDI	Class I	Active
Nar	85-2426	FDA UDI	N/A	Active
Nar	85-2930	FDA UDI	N/A	Active
Nar	80-1080	FDA UDI	N/A	Active
Nar	85-4647	FDA UDI	Class I	Active
NAR Kit	85-2505	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