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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 41 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-2813	FDA UDI	N/A	Active
Nar	85-2731	FDA UDI	N/A	Active
Nar	80-1490	FDA UDI	N/A	Active
Nar	85-3426	FDA UDI	Class I	Active
Nar	85-3331	FDA UDI	N/A	Active
Nar	85-3499	FDA UDI	N/A	Active
NAR Kit	85-2368	FDA UDI	N/A	Active
Nar	82-0075	FDA UDI	N	Active
Nar	85-4517	FDA UDI	Class I	Active
TACTICAL CricKIT	85-3680	FDA UDI	Class II	Active
NAR Kit	80-1073	FDA UDI	N/A	Active
Nar	83-0001	FDA UDI	Class II	Active
Nar	85-0093	FDA UDI	N/A	Active
Nar	85-1651	FDA UDI	N/A	Active
NAR Kit	85-0020	FDA UDI	N/A	Active
Nar	80-1827	FDA UDI	N	Active
Nar	80-1433	FDA UDI	Class I	Active
NAR Kit	85-3246	FDA UDI	N/A	Active
Nar	85-1372	FDA UDI	N/A	Active
Nar	85-3304	FDA UDI	N/A	Active
NAR Kit	80-0498	FDA UDI	N/A	Active
Nar	85-4878	FDA UDI	Class I	Active
Nar	77-0101	FDA UDI	Class I	Active
Nar	85-1571	FDA UDI	N/A	Active
NAR Kit	83-0014	FDA UDI	N/A	Active
Nar	85-2727	FDA UDI	N/A	Active
Nar	85-4677	FDA UDI	Class I	Active
Nar	85-3344	FDA UDI	N/A	Active
NAR Kit	80-0176	FDA UDI	N/A	Unknown
Nar	82-0065	FDA UDI	N	Active
Nar	85-4487	FDA UDI	N	Active
Nar	85-3142	FDA UDI	N/A	Active
NAR Kit	83-0007	FDA UDI	Class I	Active
Nar	85-2271	FDA UDI	N/A	Active
Nar	80-0889-TLS	FDA UDI	Class I	Active
Nar	84-0147	FDA UDI	Class I	Active
Nar	85-2130	FDA UDI	N/A	Active
Nar	80-1549	FDA UDI	Class I	Active
NAR kit	84-0008	FDA UDI	N/A	Active
Nar	85-4485	FDA UDI	N	Active
Nar	80-1102	FDA UDI	N/A	Active
Nar	85-2638	FDA UDI	N/A	Active
Nar	20-0118	FDA UDI	Class I	Active
Nar	85-3627	FDA UDI	N/A	Active
Nar	85-4672	FDA UDI	Class I	Active
NAR Kit	85-2486	FDA UDI	N/A	Active
Nar	85-3544	FDA UDI	N/A	Active
Nar	82-0071	FDA UDI	N	Active
Nar	85-4347	FDA UDI	Class I	Active
Nar	85-4658	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