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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

Information

Country: US
Address: 35 TEDWALL COURT, Greer, SC, 29650
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3005034064
DUNS Number: —

Catalogue (3581)

Page 40 of 72

Device	Model / Reference	Registries	Class	Status
Nar	85-3735	FDA UDI	N/A	Active
NAR Kit	85-3034	FDA UDI	N/A	Active
Nar	85-3854	FDA UDI	N/A	Active
Nar	80-1476	FDA UDI	N/A	Active
NAR Kit	85-1804	FDA UDI	N/A	Active
Nar	85-4676	FDA UDI	Class I	Active
NAR Kit	80-1203	FDA UDI	N/A	Active
Nar	85-3012	FDA UDI	N/A	Active
Nar	80-1667	FDA UDI	Class I	Active
NAR Kit	85-3608	FDA UDI	N/A	Active
Nar	80-0452	FDA UDI	N/A	Active
NAR Kit	85-1522	FDA UDI	N/A	Active
NAR Kit	85-0186	FDA UDI	N/A	Unknown
Nar	82-0047	FDA UDI	N/A	Active
Nar	85-2456	FDA UDI	N/A	Active
NAR Kit	85-2084	FDA UDI	N/A	Active
Nar	85-3081	FDA UDI	N/A	Active
Nar	85-4493	FDA UDI	Class I	Active
Nar	77-0095	FDA UDI	Class I	Active
Nar	80-0903	FDA UDI	N/A	Active
Nar	80-1752	FDA UDI	Class I	Active
Nar	80-0974	FDA UDI	N/A	Active
Nar	85-2833	FDA UDI	N/A	Active
NAR Kit	85-1401	FDA UDI	N/A	Active
Nar	85-3072	FDA UDI	N/A	Active
NAR Kit	85-2903	FDA UDI	N/A	Active
Nar	85-3091	FDA UDI	N/A	Active
Nar	85-1390	FDA UDI	N/A	Active
Nar	80-1700	FDA UDI	Class I	Active
Nar	85-4397	FDA UDI	Class I	Active
Nar	85-1803	FDA UDI	N/A	Active
Nar	85-1962	FDA UDI	N/A	Active
NAR Kit	85-2325	FDA UDI	N/A	Active
Nar	85-2134	FDA UDI	N/A	Active
Nar	85-3727	FDA UDI	N/A	Active
Nar	85-2729	FDA UDI	Class I	Active
Nar	77-0105	FDA UDI	Class I	Active
Nar	85-2900	FDA UDI	N/A	Active
Nar	85-4900	FDA UDI	Class I	Active
Nar	85-1686	FDA UDI	N/A	Active
NAR Kit	85-3692	FDA UDI	N/A	Active
Life Warmer Quantum Charger	63-5905	FDA UDI	Class II	Active
Life Warmer Quantum Thermal Transfusion Set for Blood and Blood Products (TTS-B)	63-5904	FDA UDI	Class II	Active
NAR Kit	80-0372	FDA UDI	N/A	Active
NAR Kit	85-0053	FDA UDI	N/A	Active
Nar	85-4464	FDA UDI	N	Active
Nar	85-2005	FDA UDI	Class I	Active
Nar	85-1724	FDA UDI	N/A	Active
Black Talon	ZZ-0218	FDA UDI	Class I	Active
NAR Kit	85-2653	FDA UDI	N/A	Active

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FDA Recalls (4)

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