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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 32 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-2934	FDA UDI	N/A	Active
Nar	85-1690	FDA UDI	N/A	Active
NAR Kit	82-0050	FDA UDI	N/A	Active
NAR Kit	85-3127	FDA UDI	N/A	Active
NAR Kit	80-0313	FDA UDI	N/A	Active
Nar	85-3869	FDA UDI	N/A	Active
Nar	85-1606	FDA UDI	N/A	Active
NAR Kit	85-0417	FDA UDI	N/A	Active
NAR Kit	80-0149	FDA UDI	Class I	Active
Nar	85-1371	FDA UDI	N/A	Active
NAR Kit	85-0740	FDA UDI	Class I	Active
Nar	80-1712	FDA UDI	Class I	Active
Nar	85-4084	FDA UDI	Class I	Active
Nar	85-3318	FDA UDI	N/A	Active
Nar	85-3543	FDA UDI	N/A	Active
NAR Kit	85-1029	FDA UDI	N/A	Active
NAR Kit	85-3738	FDA UDI	N/A	Active
NAR Kit	85-1778	FDA UDI	N/A	Active
NAR Kit	85-3138	FDA UDI	N/A	Active
NAR Kit	85-1499	FDA UDI	N/A	Active
NAR Kit	85-2738	FDA UDI	N/A	Active
Personal protection equipment kit	70-0007	FDA UDI	N/A	Unknown
Nar	84-0075	FDA UDI	N/A	Active
NAR Kit	80-1086	FDA UDI	N/A	Unknown
Nar	20-0101	FDA UDI	Class I	Active
Nar	85-1575	FDA UDI	N/A	Active
Nar	85-3761	FDA UDI	N/A	Active
NAR Kit	85-2905	FDA UDI	N/A	Active
Nar	80-1800	FDA UDI	Class I	Active
Nar	85-3959	FDA UDI	N/A	Active
Nar	85-4611	FDA UDI	Class I	Active
NAR Kit	80-1070	FDA UDI	N/A	Active
NAR Kit	80-0513	FDA UDI	N/A	Active
Nar	85-3027	FDA UDI	N/A	Active
Nar	85-4728	FDA UDI	Class I	Active
Nar	30-0094	FDA UDI	Class I	Active
Nar	84-0152	FDA UDI	Class I	Active
Nar	85-3985	FDA UDI	N/A	Active
Nar	85-3894	FDA UDI	N/A	Active
NAR Kit	85-2606	FDA UDI	N/A	Active
Nar	85-4363	FDA UDI	Class I	Active
Nar	80-1805	FDA UDI	N	Active
Nar	85-4166	FDA UDI	N/A	Active
Nar	85-3065	FDA UDI	N/A	Active
NAR Kit	85-1990	FDA UDI	N/A	Active
Nar	80-1618	FDA UDI	Class I	Active
NAR Kit	85-2167	FDA UDI	N/A	Active
Nar	83-0031	FDA UDI	N/A	Active
Nar	85-3730	FDA UDI	N/A	Active
Nar	80-0914	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