North American Rescue LLC.: FDA recalls

FDA enforcement reports name North American Rescue LLC. as the recalling firm in 5 events. The events have 13 product records. The recalls started from 2016 to 2026.

See the 5 events

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on 1 Oct 2026. openFDA export of 28 Sep 2026.

Enforcement events

5 events, newest first.

FDA enforcement events of North American Rescue LLC.
Initiated	Product (first record)	Type	Class	Records	Status
27 Mar 2026	AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the appropriate level provider to evaluate and treat patients at the point-of-injury / point-of-illness. The original manufacturer labeling, including single use indications, is…	Device	Class I	1	Ongoing
1 Jul 2025	JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete (Modules 1-3), REF: 85-0550; KIT, TCCC MODULE ONE - SKILLS, REF: 85-0519; KIT, MULTI MISSION EXPEDITIONARY RESPONSE - MMERK, REF: 85-2420; KIT, TCCC SKILLS/IFAK COMBO, REF: 85-0740, KIT, TCCC/TECC MODULE…	Device	Class II	1	Ongoing
27 Aug 2021	10 ga ARS Decompression Needle, Part Number ZZ-0298	Device	Class II	1	Terminated
21 Aug 2020	4 In. Flat Responder Emergency Trauma Dressing part number 30-0171, packaged in kits labeled as follows: a) M-FAK Mini First Aid Kit; Kit Product Code: 80-0890 b) M-FAK Mini First Aid Kit, with Bleeding Control Dressing; Kit Product Code: 80-0891 c) M-FAK Mini First Aid Kit, Advance; Kit Product Code: 80-0892 d)…	Device	Class II	1	Terminated
27 Sep 2016	Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue	Drug	Class II	9	Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Follow by RSS:Food, drug and device recallsFDA Class I recalls

Type and class

North American Rescue LLC.: events for each product type
Type		Events
Device		4
Drug		1

North American Rescue LLC.: events in each class
Class		Events
Class II		4
Class I		1

Share of the events of the firm in Class I: 20%
Share of all events on the register in Class I: 18%
Events with the status Ongoing: 2

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of North American Rescue LLC., by the year that the recall started. The largest year is 2016, with 1 event.

Official channels

FDA enforcement reportsThe FDA search of the weekly enforcement reports.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA: report a problemThe FDA page that shows where a report about a product goes.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

Cite this page

Recall Register. North American Rescue LLC.: FDA recalls. https://recallregister.com/firm/north-american-rescue-llc/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

Source: openFDA enforcement reports
Licence: CC0 1.0
Export date: 28 Sep 2026
State of the firm address: SC

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of North American Rescue LLC. have?: Class II: 4 events. Class I: 1 event. The class is for the product of a recall. It is not a class of the firm.
Which product types do the FDA recalls of North American Rescue LLC. have?: Device: 4 events. Drug: 1 event.
What is the newest FDA recall of North American Rescue LLC.?: FDA event 98697, which the firm started on 27 Mar 2026. The first product in the record is: AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the appropriate level provider to evaluate and treat patients at the point-of-injury / point-of-illness. The original manufacturer labeling, including single use indications, is…
How many FDA recalls of North American Rescue LLC. have the status Ongoing?: 2 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.