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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 34 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-3990	FDA UDI	N/A	Active
NAR Kit	85-3033	FDA UDI	N/A	Active
Nar	10-0029	FDA UDI	Class I	Active
Nar	85-4608	FDA UDI	Class I	Active
Nar	80-1105	FDA UDI	N/A	Active
NAR Kit	85-1663	FDA UDI	N/A	Active
NAR Kit	85-0706	FDA UDI	N/A	Active
Nar	85-4892	FDA UDI	Class I	Active
Nar	85-2549	FDA UDI	N/A	Active
Nar	80-1771	FDA UDI	Class I	Active
Nar	85-4214	FDA UDI	Class I	Active
Nar	85-4946	FDA UDI	Class I	Active
Nar	85-4854	FDA UDI	Class I	Active
Nar	85-3095	FDA UDI	N/A	Active
Life Warmer Quantum Controller	63-5901	FDA UDI	Class II	Active
Nar	85-4381	FDA UDI	Class I	Active
Nar	85-4245	FDA UDI	N/A	Active
Nar	85-4690	FDA UDI	Class I	Active
Nar	85-3936	FDA UDI	N/A	Active
Nar	80-1546	FDA UDI	Class I	Active
Nar	85-2070	FDA UDI	N/A	Active
Nar	85-3397	FDA UDI	N/A	Active
Nar	85-1691	FDA UDI	N/A	Active
Nar	85-4311	FDA UDI	Class I	Active
NAR Kit	85-2757	FDA UDI	N/A	Active
Nar	85-1582	FDA UDI	N/A	Active
Nar	80-0525	FDA UDI	N/A	Active
Nar	80-0522	FDA UDI	N/A	Active
Nar	80-1674	FDA UDI	Class I	Active
Nar	85-4629	FDA UDI	Class I	Active
Nar	85-2880	FDA UDI	N/A	Active
Nar	85-3861	FDA UDI	N/A	Active
Nar	85-3887	FDA UDI	N/A	Active
Nar	85-4028	FDA UDI	Class I	Active
Nar	80-0998	FDA UDI	N/A	Active
NAR Kit	85-1360	FDA UDI	N/A	Active
Nar	85-3595	FDA UDI	N/A	Active
Nar	85-1507	FDA UDI	N/A	Active
NAR Kit	80-1076	FDA UDI	N/A	Active
Nar	85-3853	FDA UDI	N/A	Active
NAR Kit	85-2350	FDA UDI	N/A	Active
Nar	80-1049	FDA UDI	N/A	Active
NAR Kit	85-2804	FDA UDI	N/A	Active
Nar	85-3707	FDA UDI	N/A	Active
Nar	80-1444	FDA UDI	N/A	Active
Nar	85-4220	FDA UDI	N/A	Active
Nar	85-2192	FDA UDI	N/A	Active
NAR Kit	85-2780	FDA UDI	N/A	Active
Nar	85-4863	FDA UDI	Class I	Active
Nar	85-4964	FDA UDI	Class I	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