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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 30 of 72

Device	Model / Reference	Registries	Class	Status
NAR Kit	85-1525	FDA UDI	N/A	Active
Nar	85-2195	FDA UDI	N/A	Active
Nar	85-1992	FDA UDI	N/A	Active
Nar	85-0777	FDA UDI	N/A	Active
Nar	85-4131	FDA UDI	N/A	Active
Nar	85-3221	FDA UDI	N/A	Active
Nar	85-1802	FDA UDI	N/A	Active
Nar	85-2310	FDA UDI	N/A	Active
Nar	85-4238	FDA UDI	N/A	Active
Nar	85-4876	FDA UDI	Class I	Active
NAR Kit	85-1787	FDA UDI	N/A	Active
Nar	80-1668	FDA UDI	Class I	Active
Nar	88-0034	FDA UDI	Class I	Active
Nar	84-0168	FDA UDI	Class I	Active
Nar	85-3739	FDA UDI	N/A	Active
Nar	85-3005	FDA UDI	N/A	Active
Nar	85-3763	FDA UDI	N/A	Active
NAR Kit	80-0135	FDA UDI	N/A	Active
NAR Kit	85-2910	FDA UDI	N/A	Active
Nar	85-3871	FDA UDI	N/A	Active
NAR Kit	85-1763	FDA UDI	N/A	Unknown
Nar	85-2110	FDA UDI	N/A	Active
NAR Kit	85-0795	FDA UDI	N/A	Active
NAR Kit	85-1349	FDA UDI	N/A	Active
Nar	85-4734	FDA UDI	Class I	Active
NAR Kit	80-1167	FDA UDI	N/A	Active
Nar	88-0002	FDA UDI	Class I	Active
Nar	85-2755	FDA UDI	N/A	Active
Nar	85-2942	FDA UDI	N/A	Active
Nar	85-1777	FDA UDI	N/A	Active
Nar	80-1772	FDA UDI	Class I	Active
NAR Kit	85-1097	FDA UDI	N/A	Active
Nar	85-2911	FDA UDI	N/A	Active
NAR Kit	85-2840	FDA UDI	N/A	Active
Nar	85-0332	FDA UDI	N/A	Active
NAR Kit	85-1262	FDA UDI	N/A	Active
Nar	85-2654	FDA UDI	N/A	Active
Nar	85-4484	FDA UDI	Class I	Active
NAR Kit	80-1060	FDA UDI	N/A	Active
Nar	80-1474	FDA UDI	N/A	Active
Nar	85-1798	FDA UDI	N/A	Active
NAR Kit	85-2676	FDA UDI	N/A	Active
Nar	85-3584	FDA UDI	N/A	Active
NAR Kit	80-1211	FDA UDI	N/A	Active
Nar	80-1714	FDA UDI	Class I	Active
NAR Kit	84-0024	FDA UDI	N/A	Active
Nar	85-4197	FDA UDI	N/A	Active
NAR Kit	85-2690	FDA UDI	N/A	Active
Nar	84-0091	FDA UDI	N/A	Active
TACTICAL CricKIT	85-4469	FDA UDI	Class II	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