Is this your brand? Sign in to claim ownership.

NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Page 45 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-4688-TLS	FDA UDI	Class I	Active
Nar	80-1813	FDA UDI	Class I	Active
Nar	80-0937	FDA UDI	N/A	Active
NAR Kit	85-1328	FDA UDI	N/A	Active
NAR Kit	85-2620	FDA UDI	N/A	Active
NAR Kit	85-2803	FDA UDI	N/A	Active
Nar	85-3992	FDA UDI	N/A	Active
NAR Kit	85-3141	FDA UDI	N/A	Active
NAR Kit	84-0089	FDA UDI	N/A	Active
NAR Kit	85-1397	FDA UDI	N/A	Active
Nar	85-3900	FDA UDI	N/A	Active
NAR Kit	80-1072	FDA UDI	N/A	Active
Nar	80-1547	FDA UDI	Class I	Active
Nar	85-4480	FDA UDI	N	Active
Nar	80-1823	FDA UDI	N	Active
Nar	85-3129	FDA UDI	N/A	Active
NAR kit	84-0003	FDA UDI	N/A	Active
Nar	85-2164	FDA UDI	N/A	Active
Nar	80-1221	FDA UDI	N/A	Active
Nar	80-1745	FDA UDI	Class I	Active
Nar	85-1375	FDA UDI	N/A	Active
Nar	85-2071-TLS	FDA UDI	Class I	Active
NAR Kit	80-0107	FDA UDI	N/A	Active
NAR Kit	85-1931	FDA UDI	N/A	Active
Nar	85-1426	FDA UDI	N/A	Active
NAR Kit	80-0565	FDA UDI	N/A	Active
Nar	85-3798	FDA UDI	N/A	Active
Nar	85-4938	FDA UDI	Class I	Active
NAR Kit	80-0249	FDA UDI	N/A	Active
NAR Kit	85-0874	FDA UDI	N/A	Active
NAR Kit	85-0339	FDA UDI	N/A	Active
Nar	80-1219	FDA UDI	Class I	Active
Nar	85-4569	FDA UDI	N	Active
NAR Kit	80-1094	FDA UDI	N/A	Active
Nar	85-1553	FDA UDI	N/A	Active
NAR Kit	85-1345	FDA UDI	N/A	Active
Nar	85-2307	FDA UDI	N/A	Active
NAR Kit	84-0022	FDA UDI	N/A	Active
NAR Kit	85-1602	FDA UDI	N/A	Unknown
NAR Kit	85-3562	FDA UDI	N/A	Active
Nar	80-1557	FDA UDI	N/A	Active
Nar	80-1677	FDA UDI	Class I	Active
Nar	85-4165	FDA UDI	N/A	Active
Nar	85-4240	FDA UDI	N/A	Active
Nar	85-3942	FDA UDI	N/A	Active
Nar	85-1612	FDA UDI	N/A	Active
Nar	80-0542	FDA UDI	N/A	Active
Nar	85-2598	FDA UDI	N/A	Active
Nar	85-2127	FDA UDI	N/A	Active
Nar	85-2482	FDA UDI	N/A	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