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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 20 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-4170	FDA UDI	Class I	Active
Nar	85-4471	FDA UDI	Class I	Active
Nar	85-3974	FDA UDI	N/A	Active
NAR Kit	85-2189	FDA UDI	N/A	Active
NAR Kit	80-1144	FDA UDI	N/A	Active
NAR Kit	85-3424	FDA UDI	N/A	Active
Nar	85-2223	FDA UDI	N/A	Active
Nar	84-0166-TLS	FDA UDI	Class I	Active
NAR Kit	85-1638	FDA UDI	N/A	Active
NAR Kit	80-0549	FDA UDI	N/A	Active
NAR Kit	85-1346	FDA UDI	N/A	Active
NAR Kit	85-3487	FDA UDI	N/A	Active
NAR Kit	85-1648	FDA UDI	N/A	Active
Nar	85-4614	FDA UDI	Class I	Active
Nar	85-1184	FDA UDI	N/A	Active
Nar	85-3046	FDA UDI	N/A	Active
NAR Kit	85-2150	FDA UDI	N/A	Active
Nar	85-2176	FDA UDI	N/A	Active
NAR Kit	83-0012	FDA UDI	N/A	Active
NAR Kit	80-0174	FDA UDI	N/A	Unknown
Nar	85-4092	FDA UDI	N/A	Active
Nar	82-0081	FDA UDI	N	Active
Nar	85-4523	FDA UDI	Class I	Active
Nar	85-2933	FDA UDI	N/A	Active
NAR Kit	83-0013	FDA UDI	N/A	Active
Nar	80-1506	FDA UDI	N/A	Active
Nar	85-3891	FDA UDI	N/A	Active
Nar	85-3066	FDA UDI	N/A	Active
NAR Kit	85-1413	FDA UDI	N/A	Active
NAR Kit	80-0295	FDA UDI	N/A	Unknown
Nar	85-4653	FDA UDI	Class I	Active
Nar	85-1845	FDA UDI	N/A	Active
NAR Kit	85-1684	FDA UDI	N/A	Active
Nar	30-0167	FDA UDI	Class I	Active
Nar	85-3786	FDA UDI	N/A	Active
NAR Kit	82-0049	FDA UDI	N/A	Active
NAR Kit	85-2179	FDA UDI	N/A	Active
NAR Kit	85-1938	FDA UDI	N/A	Active
Nar	85-2065	FDA UDI	N/A	Active
Nar	85-3585	FDA UDI	N/A	Active
Nar	80-0139	FDA UDI	Class I	Active
Nar	85-2063	FDA UDI	N/A	Active
Nar	85-1011	FDA UDI	N/A	Active
NAR Kit	ZZ-0424	FDA UDI	N/A	Active
Nar	80-1634	FDA UDI	Class I	Active
NAR Kit	80-1092	FDA UDI	N/A	Active
NAR Kit	85-2078	FDA UDI	N/A	Active
Nar	85-4907	FDA UDI	Class I	Active
Nar	85-4415	FDA UDI	Class I	Active
Nar	85-4221	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