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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 35 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-4383	FDA UDI	Class I	Active
Nar	85-4143	FDA UDI	N/A	Active
Nar	85-4302	FDA UDI	N	Active
Nar	85-2400	FDA UDI	N/A	Active
Nar	85-2530	FDA UDI	N/A	Active
Nar	77-0104	FDA UDI	Class I	Active
Nar	85-3726	FDA UDI	N/A	Active
Nar	80-1773	FDA UDI	N	Active
Nar	80-1695	FDA UDI	Class I	Active
Nar	85-3676	FDA UDI	N/A	Active
NAR Kit	80-1190	FDA UDI	N/A	Active
Nar	85-0918	FDA UDI	N/A	Active
Nar	85-3905	FDA UDI	N/A	Active
Nar	80-0580	FDA UDI	N/A	Active
Nar	85-1513	FDA UDI	N/A	Active
NAR Kit	85-0185	FDA UDI	N/A	Unknown
NAR Kit	85-2539	FDA UDI	N/A	Active
TACTICAL CricKIT	10-0017-NB	FDA UDI	Class II	Active
Nar	85-1955	FDA UDI	N/A	Active
NAR Kit	85-3446	FDA UDI	N/A	Active
Nar	85-0413	FDA UDI	N/A	Active
Nar	85-4242	FDA UDI	N/A	Unknown
Nar	85-1932	FDA UDI	N/A	Active
Nar	80-1450	FDA UDI	N/A	Active
Nar	85-3464	FDA UDI	N/A	Active
Nar	85-4423	FDA UDI	Class I	Active
Nar	85-4838	FDA UDI	N	Active
NAR Kit	85-1552	FDA UDI	N/A	Active
Nar	85-2921	FDA UDI	N/A	Active
Nar	85-4556	FDA UDI	Class I	Active
Nar	85-4665	FDA UDI	Class I	Active
NAR Kit	85-3040	FDA UDI	N/A	Active
Nar	85-4729	FDA UDI	Class I	Active
Nar	85-4102	FDA UDI	N/A	Active
Nar	80-1479	FDA UDI	N/A	Active
NAR Kit	85-0367	FDA UDI	N/A	Active
Nar	80-1787	FDA UDI	Class I	Active
NAR Kit	80-0310	FDA UDI	N/A	Active
Nar	84-0180	FDA UDI	Class I	Active
NAR Kit	80-1045	FDA UDI	N/A	Active
Nar	85-3545	FDA UDI	N/A	Active
NAR Kit	85-3455	FDA UDI	N/A	Active
Nar	77-0106	FDA UDI	Class I	Active
Nar	85-1392	FDA UDI	Class I	Active
NAR Kit	85-1700	FDA UDI	N/A	Active
Nar	80-1065	FDA UDI	N/A	Active
Nar	85-3731	FDA UDI	N/A	Active
Nar	85-3922	FDA UDI	N/A	Active
NAR Kit	20-0057	FDA UDI	N/A	Active
NAR Kit	80-1231	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