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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 54 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-3453	FDA UDI	N/A	Active
Nar	85-3812	FDA UDI	N/A	Active
Nar	85-4004	FDA UDI	Class I	Active
Nar	85-1722	FDA UDI	N/A	Active
Nar	85-4930	FDA UDI	Class I	Active
NAR Kit	85-1541	FDA UDI	N/A	Active
Nar	85-4802	FDA UDI	N	Active
NAR Kit	85-1726	FDA UDI	N/A	Unknown
Nar	85-4544	FDA UDI	Class I	Active
Nar	80-1704	FDA UDI	Class I	Active
Nar	80-0872	FDA UDI	N/A	Active
Nar	80-1508	FDA UDI	N/A	Active
Nar	85-2785	FDA UDI	N/A	Active
NAR Kit	85-1415	FDA UDI	N/A	Active
NAR Kit	85-1075	FDA UDI	N/A	Active
NAR Kit	80-1047	FDA UDI	N/A	Active
Nar	85-4123	FDA UDI	N/A	Active
NAR Kit	85-1652	FDA UDI	N/A	Active
NAR Kit	85-3406	FDA UDI	N/A	Active
Nar	85-3486	FDA UDI	N/A	Active
Nar	85-4820	FDA UDI	Class I	Active
Nar	85-2786	FDA UDI	N/A	Active
Nar	85-2436	FDA UDI	N/A	Active
NAR Kit	80-1176	FDA UDI	N/A	Active
Nar	60-0008	FDA UDI	Class I	Active
Nar	85-3535	FDA UDI	N/A	Active
NAR Kit	80-0364	FDA UDI	N/A	Unknown
Nar	85-3743	FDA UDI	N/A	Active
NAR Kit	85-2745	FDA UDI	N/A	Active
Nar	85-1688	FDA UDI	N/A	Active
Nar	80-1218	FDA UDI	N/A	Active
NAR Kit	80-0500	FDA UDI	N/A	Active
NAR Kit	85-0197	FDA UDI	N/A	Active
Nar	85-4503	FDA UDI	Class I	Active
Nar	85-3842	FDA UDI	N/A	Active
Nar	80-0135-TLS	FDA UDI	Class I	Active
NAR Kit	85-0181	FDA UDI	N/A	Unknown
Nar	85-4942	FDA UDI	Class I	Active
Nar	80-1446	FDA UDI	N/A	Active
Nar	85-1297	FDA UDI	N/A	Active
Nar	30-0052	FDA UDI	Class I	Active
Nar	85-3491	FDA UDI	N/A	Active
Nar	85-1357	FDA UDI	N/A	Active
NAR Kit	85-1373	FDA UDI	N/A	Active
NAR Kit	85-2602	FDA UDI	N/A	Active
NAR Kit	85-2247	FDA UDI	N/A	Active
Nar	85-4140	FDA UDI	N/A	Active
Nar	80-1558	FDA UDI	N	Active
Nar	80-1482	FDA UDI	N/A	Active
Nar	80-1125	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