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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 37 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-3548	FDA UDI	N/A	Active
NAR Kit	10-0027	FDA UDI	Class I	Active
Nar	80-1475	FDA UDI	N/A	Active
Nar	77-0092	FDA UDI	Class I	Active
Nar	85-2817	FDA UDI	N/A	Active
Nar	85-3741	FDA UDI	N/A	Active
Nar	80-0573	FDA UDI	N/A	Active
Nar	82-0029	FDA UDI	N/A	Active
Nar	85-4230	FDA UDI	N/A	Active
Nar	85-4050	FDA UDI	N/A	Active
Nar	85-4035	FDA UDI	N/A	Active
Nar	85-1487	FDA UDI	N/A	Active
Life Warmer Quantum Blood and Fluid Warming System	63-5900	FDA UDI	Class II	Active
NAR Kit	85-1497	FDA UDI	N/A	Active
Nar	80-1654	FDA UDI	Class I	Active
Nar	85-3229	FDA UDI	N/A	Active
NAR Kit	85-2693	FDA UDI	N/A	Active
NAR Kit	80-0039	FDA UDI	N/A	Active
NAR Kit	80-0173	FDA UDI	N/A	Active
Nar	85-4348	FDA UDI	Class I	Active
Nar	85-1352	FDA UDI	N/A	Active
Nar	85-3466	FDA UDI	N/A	Active
NAR Kit	85-3467	FDA UDI	N/A	Active
Nar	85-3823	FDA UDI	N/A	Unknown
Nar	80-0579	FDA UDI	N/A	Active
Nar	85-4804	FDA UDI	N	Active
Nar	77-0081	FDA UDI	Class I	Active
Nar	85-3300	FDA UDI	N/A	Active
Nar	85-1136	FDA UDI	N/A	Active
Nar	85-2941	FDA UDI	N/A	Active
Nar	85-2988	FDA UDI	N/A	Active
NAR Kit	85-1707	FDA UDI	N/A	Active
Nar	80-0527	FDA UDI	N/A	Active
Nar	85-3117	FDA UDI	N/A	Active
NAR Kit	80-0005	FDA UDI	N/A	Active
Nar	85-2781	FDA UDI	N/A	Active
NAR Kit	80-0202	FDA UDI	N/A	Active
Nar	85-4512	FDA UDI	N	Active
Nar	85-2327	FDA UDI	N/A	Active
NAR Kit	80-0445	FDA UDI	N/A	Active
Nar	85-3849	FDA UDI	N/A	Active
NAR Kit	80-0319	FDA UDI	N/A	Unknown
Nar	85-3188	FDA UDI	N/A	Active
Nar	85-2728	FDA UDI	N/A	Active
Nar	80-1560	FDA UDI	N/A	Active
Nar	85-3541	FDA UDI	N/A	Active
Nar	85-2526	FDA UDI	N/A	Active
Nar	85-3917	FDA UDI	N/A	Active
NAR Kit	85-1605	FDA UDI	N/A	Active
Nar	80-1454	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