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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 46 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-1584	FDA UDI	N/A	Active
Nar	85-4372	FDA UDI	Class I	Active
Nar	85-4882	FDA UDI	Class I	Active
NAR Kit	85-3518	FDA UDI	N/A	Active
Nar	80-1635	FDA UDI	Class I	Active
Nar	85-3020	FDA UDI	N/A	Active
NAR Kit	85-0012	FDA UDI	N/A	Active
Nar	85-2013	FDA UDI	N/A	Active
NAR Kit	80-0288	FDA UDI	N/A	Active
NAR Kit	85-2300	FDA UDI	N/A	Active
NAR Kit	80-0279	FDA UDI	N/A	Unknown
NAR Kit	85-1364	FDA UDI	N/A	Active
Nar	80-1548	FDA UDI	Class I	Active
Nar	85-3307	FDA UDI	N/A	Active
Nar	84-0144	FDA UDI	Class I	Active
Nar	85-4187	FDA UDI	N/A	Active
NAR Kit	80-1003	FDA UDI	N/A	Active
NAR Kit	85-1640	FDA UDI	N/A	Active
Nar	80-0965	FDA UDI	N/A	Active
Nar	85-4870	FDA UDI	Class I	Active
NAR Kit	85-3380	FDA UDI	N/A	Active
Nar	85-1491	FDA UDI	N/A	Active
Nar	85-0437	FDA UDI	Class I	Active
Nar	85-2085	FDA UDI	N/A	Active
Nar	88-0018	FDA UDI	Class I	Active
Nar	85-3437	FDA UDI	N/A	Active
Nar	85-2832	FDA UDI	N/A	Active
Nar	85-4766	FDA UDI	Class I	Active
Nar	85-2226	FDA UDI	N/A	Active
NAR Kit	85-2155	FDA UDI	N/A	Unknown
Nar	85-3289	FDA UDI	N/A	Active
Nar	85-3162	FDA UDI	N/A	Active
Nar	84-0183	FDA UDI	Class I	Active
NAR Kit	85-2680	FDA UDI	N/A	Active
Nar	85-2877	FDA UDI	N/A	Active
Nar	85-1751	FDA UDI	N/A	Active
Nar	85-4369	FDA UDI	N	Active
Nar	85-2595	FDA UDI	N/A	Active
Nar	85-2622	FDA UDI	N/A	Active
NAR Kit	80-0458	FDA UDI	N/A	Active
NAR Kit	85-3472	FDA UDI	N/A	Active
Nar	85-1477	FDA UDI	N/A	Active
NAR Kit	85-1518	FDA UDI	N/A	Active
Nar	85-2004	FDA UDI	N/A	Active
NAR Kit	85-1320	FDA UDI	N/A	Active
Nar	85-4903	FDA UDI	Class I	Active
NAR Kit	85-0897	FDA UDI	N/A	Active
NAR Kit	80-0134	FDA UDI	N/A	Active
NAR Kit	85-0942	FDA UDI	N/A	Active
Nar	85-3908	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