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NORTH AMERICAN RESCUE, LLC.

Last updated September 17, 2026

What NORTH AMERICAN RESCUE, LLC. makes

North American Rescue, LLC. manufactures first aid kits (both non-medicated and medicated), first aid absorbent pads and bandages, arterial tourniquets (manual, single-use), cricothyrotomy kits (single-use), pneumothorax catheter insertion sets, in-line backflow valves (single-use), and nasopharyngeal airways (single-use).

The company's devices are classified as Class I, Class II, and N, and are listed in the FDA UDI registry. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of devices does North American Rescue, LLC. manufacture?

Where is North American Rescue, LLC. based?

North American Rescue, LLC. is based in the United States, as explicitly stated in the COMPANY and COUNTRY fields of the provided data.

In which regulatory registry are North American Rescue, LLC.'s devices listed?

North American Rescue, LLC.'s devices are listed in the FDA UDI registry, as indicated by the LISTED IN field in the provided data.

How are the devices manufactured by North American Rescue, LLC. classified?

The devices manufactured by North American Rescue, LLC. are classified as Class I, Class II, and N, as stated in the DEVICE CLASSES field of the provided data.

AI-generated from registry data and not verified by a human reviewer.

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 1 of 72

Device	Model / Reference	Registries	Class	Status
Nar	80-0865	FDA UDI	N/A	Active
Nar	80-1138	FDA UDI	N/A	Active
Nar	80-1686	FDA UDI	Class I	Active
Nar	85-1586	FDA UDI	Class I	Active
Nar	85-4068	FDA UDI	N/A	Active
Nar	85-3978	FDA UDI	N/A	Active
Nar	85-3339	FDA UDI	N/A	Active
NAR Kit	85-3414	FDA UDI	N/A	Active
Nar	85-4692	FDA UDI	Class I	Active
Nar	85-3935	FDA UDI	N/A	Active
Nar	85-2149	FDA UDI	N/A	Active
Nar	85-2114	FDA UDI	N/A	Active
NAR Kit	85-1842	FDA UDI	N/A	Active
Nar	85-3829	FDA UDI	N/A	Active
Nar	85-4810	FDA UDI	Class I	Active
NAR Kit	85-2778	FDA UDI	N/A	Active
Nar	85-3120	FDA UDI	N/A	Active
Nar	85-2714	FDA UDI	N/A	Active
Nar	85-2811	FDA UDI	N/A	Active
NAR Kit	85-2256	FDA UDI	N/A	Active
Nar	85-2080	FDA UDI	N/A	Active
Nar	80-0583	FDA UDI	N/A	Active
Nar	85-1620	FDA UDI	N/A	Active
Nar	85-4630	FDA UDI	Class I	Active
Nar	83-0002	FDA UDI	Class II	Active
Nar	85-4442	FDA UDI	Class I	Active
Nar	85-3150	FDA UDI	N/A	Active
Nar	83-0039	FDA UDI	Class I	Active
Nar	85-4392	FDA UDI	Class I	Active
NAR Kit	85-3416	FDA UDI	N/A	Active
NAR Kit	85-1145	FDA UDI	N/A	Active
Nar	80-0497	FDA UDI	N/A	Active
Nar	85-2917	FDA UDI	N/A	Active
Nar	85-1974	FDA UDI	N/A	Active
Nar	85-4305	FDA UDI	Class I	Active
Nar	85-2466	FDA UDI	N/A	Active
NAR Kit	85-3032	FDA UDI	N/A	Active
NAR Kit	85-2103	FDA UDI	N/A	Active
Nar	85-1044	FDA UDI	N/A	Active
Nar	85-4186	FDA UDI	N/A	Active
NAR Kit	85-1306	FDA UDI	N/A	Active
NAR Kit	70-0216	FDA UDI	N/A	Active
Nar	85-1246	FDA UDI	N/A	Active
Nar	85-1331	FDA UDI	N/A	Active
Nar	85-3821	FDA UDI	N/A	Active
Nar	85-4579	FDA UDI	Class I	Active
Nar	85-3427	FDA UDI	Class I	Active
NAR Kit	85-2568	FDA UDI	N/A	Active
Nar	80-1594	FDA UDI	N	Active
Nar	85-4265	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

Not available yet.

Authorities

Not available yet.

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.

There are 4 recall records for NORTH AMERICAN RESCUE, LLC., with the earliest initiated on 2020-08-21 and the most recent on 2026-03-27. The statuses recorded across these recalls are open, classified, and terminated. The reasons given include: kits containing a recalled blood glucose system due to an E-5 error code related to software design for high glucose events or test strip errors; incorrect Instructions for Use included with the device; a potential manufacturing defect in a device used for limb occlusion that may compromise structural integrity and performance; and lack of sterility assurance for the 30-0171 device.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

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