North American Rescue JETT Device Recalled for Potential Manufacturing Defect

Agency Publication Date: September 26, 2025

Summary

North American Rescue LLC. is recalling 552 units of the Junctional Emergency Treatment Tool (JETT) due to a potential manufacturing defect. This medical device, which is used to stop blood flow to the lower limbs in emergency situations, may have compromised structural integrity that can lead to failure during use. The recall includes both standalone JETT units and several emergency medical and training kits where the tool is included as a component.

Risk

The defect could cause the device to break or lose its ability to compress arteries properly. If this occurs during a life-threatening emergency, it may fail to stop severe bleeding, which can lead to significant blood loss or death.

What You Should Do

The recalled product is the Junctional Emergency Treatment Tool (JETT), model REF: 30-0088, which is also distributed within various medical training and emergency kits including TCCC Training, TCCC Skills, and Multi-Mission Expeditionary Response kits.
Identify if your device or kit is affected by checking the lot number and model number printed on the product label. See the Affected Products section below for the full list of affected codes.
Stop using the recalled medical device immediately and quarantine any affected inventory.
Contact North American Rescue LLC. or your medical supply distributor to arrange for the return, replacement, or correction of the device.
Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional assistance or information regarding this recall.

Your Remedy Options

Other Action

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT)

Model / REF:

30-0088

Lot Numbers:

021224-1

81722-1

81722-2

121323-1

UDI:

00842209100002

Component inside various medical kits; also sold standalone.

Product: KIT, TCCC Training- Complete (Modules 1-3)

Model / REF:

85-0550

Lot Numbers:

85-0550091824

85-0550090424

85-0550030725

85-0550052925

85-0550052325

85-0550082324

85-0550080624

85-0550062624

85-0550052124

85-0550111424

85-0550102924

UDI:

00842209110711

Product: KIT, TCCC MODULE ONE - SKILLS

Model / REF:

85-0519

Lot Numbers:

85-0519090324

85-0519081924

UDI:

00842209110742

Product: KIT, MULTI MISSION EXPEDITIONARY RESPONSE - MMERK

Model / REF:

85-2420

Lot Numbers:

85-2420041725

85-2420042125

85-2420100324

UDI:

00842209113910

Product: KIT, TCCC SKILLS/IFAK COMBO

Model / REF:

85-0740

Lot Numbers:

85-0740042925

85-0740050625

85-0740052925

85-0740081224

85-0740082924

85-0740011325

85-0740122324

85-0740121724

85-0740112024

85-0740110424

85-0740102524

UDI:

00842209110599

Product: KIT, TCCC/TECC MODULE ONE SKILLS REFILL

Model / REF:

85-1900

Lot Numbers:

85-1900082124

85-1900031125

UDI:

00842209110810

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 97308

Status: Active

Manufacturer: North American Rescue LLC.

Sold By: Authorized distributors; Specialty medical retailers

Manufactured In: United States

Units Affected: 552

Distributed To: South Carolina, Oklahoma, Idaho, Kentucky, Virginia, Nevada, Illinois, Texas, California, Florida, Louisiana, New York, Maine, Pennsylvania, Arkansas, Arizona, Alabama, Delaware, Massachusetts, Mississippi, Hawaii, Washington, Michigan, Georgia, New Jersey, Utah, Maryland, Oregon, North Carolina

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Summary

What You Should Do

The recalled product is the Junctional Emergency Treatment Tool (JETT), model REF: 30-0088, which is also distributed within various medical training and emergency kits including TCCC Training, TCCC Skills, and Multi-Mission Expeditionary Response kits.

Identify if your device or kit is affected by checking the lot number and model number printed on the product label. See the Affected Products section below for the full list of affected codes.

Stop using the recalled medical device immediately and quarantine any affected inventory.

Contact North American Rescue LLC. or your medical supply distributor to arrange for the return, replacement, or correction of the device.

Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional assistance or information regarding this recall.

Affected Products

Product: JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT)

Model / REF:

30-0088

Lot Numbers:

021224-1

81722-1

81722-2

121323-1

UDI:

00842209100002

Component inside various medical kits; also sold standalone.

Product: KIT, TCCC Training- Complete (Modules 1-3)

Model / REF:

85-0550

Lot Numbers:

85-0550091824

85-0550090424

85-0550030725

85-0550052925

85-0550052325

85-0550082324

85-0550080624

85-0550062624

85-0550052124

85-0550111424

85-0550102924

UDI:

00842209110711

Product: KIT, TCCC MODULE ONE - SKILLS

Model / REF:

85-0519

Lot Numbers:

85-0519090324

85-0519081924

UDI:

00842209110742

Product: KIT, MULTI MISSION EXPEDITIONARY RESPONSE - MMERK

Model / REF:

85-2420

Lot Numbers:

85-2420041725

85-2420042125

85-2420100324

UDI:

00842209113910

Product: KIT, TCCC SKILLS/IFAK COMBO

Model / REF:

85-0740

Lot Numbers:

85-0740042925

85-0740050625

85-0740052925

85-0740081224

85-0740082924

85-0740011325

85-0740122324

85-0740121724

85-0740112024

85-0740110424

85-0740102524

UDI:

00842209110599

Product: KIT, TCCC/TECC MODULE ONE SKILLS REFILL

Model / REF:

85-1900

Lot Numbers:

85-1900082124

85-1900031125

UDI:

00842209110810

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 97308

Status: Active

Manufacturer: North American Rescue LLC.

Sold By: Authorized distributors; Specialty medical retailers

Manufactured In: United States

Units Affected: 552