Is this your brand? Sign in to claim ownership.

NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 23 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-4127	FDA UDI	N/A	Active
NAR Kit	85-3068	FDA UDI	N/A	Active
Nar	80-1804	FDA UDI	N	Active
Nar	80-1445	FDA UDI	N/A	Active
Nar	20-0020	FDA UDI	Class I	Active
NAR Kit	85-1758	FDA UDI	N/A	Active
Nar	85-1621	FDA UDI	N/A	Active
Nar	80-1713	FDA UDI	Class I	Active
Nar	85-2075	FDA UDI	N/A	Active
Nar	85-4913	FDA UDI	Class I	Active
Nar	85-4258	FDA UDI	N/A	Active
NAR Kit	85-2397	FDA UDI	N/A	Active
Nar	85-2384	FDA UDI	N/A	Active
Nar	85-4263	FDA UDI	Class I	Active
Nar	85-4342	FDA UDI	Class I	Active
Nar	85-4814	FDA UDI	Class I	Active
Nar	85-4716	FDA UDI	N	Active
Nar	85-4307	FDA UDI	Class I	Active
Nar	85-3449	FDA UDI	N/A	Active
Nar	85-2073	FDA UDI	N/A	Active
Nar	85-4780	FDA UDI	Class I	Active
NAR Kit	85-3154	FDA UDI	N/A	Active
Nar	85-2035	FDA UDI	N/A	Active
Nar	80-1443	FDA UDI	N/A	Active
Nar	85-4775	FDA UDI	Class I	Active
Nar	80-1457	FDA UDI	Class I	Active
NAR Kit	85-1720	FDA UDI	N/A	Active
NAR Kit	85-3312	FDA UDI	N/A	Active
NAR Kit	85-2204	FDA UDI	N/A	Active
Nar	85-4310	FDA UDI	Class I	Active
Nar	85-4483	FDA UDI	Class I	Active
NAR Kit	85-1769	FDA UDI	N/A	Active
NAR Kit	85-1047	FDA UDI	N/A	Active
Nar	85-2089	FDA UDI	N/A	Active
Nar	85-2454	FDA UDI	N/A	Active
Nar	80-0097-EU	FDA UDI	N/A	Active
Nar	85-2892	FDA UDI	N/A	Active
Nar	85-4777	FDA UDI	Class I	Active
NAR Kit	85-1548	FDA UDI	N/A	Active
Nar	85-4122	FDA UDI	N/A	Active
Nar	85-3640	FDA UDI	N/A	Active
Nar	85-2143	FDA UDI	N/A	Active
NAR Kit	85-2066	FDA UDI	N/A	Active
Nar	80-1698	FDA UDI	Class I	Active
Nar	85-4026	FDA UDI	N/A	Active
Nar	85-4505	FDA UDI	Class I	Active
NAR Kit	80-0303	FDA UDI	N/A	Active
Nar	80-1707	FDA UDI	Class I	Active
Nar	85-3828	FDA UDI	N/A	Active
Nar	85-4476	FDA UDI	Class I	Active

No authorised representatives on record.

Not available yet.

Not available yet.

Not available yet.

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