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Use caution Medical device recall · FDA · Published July 1, 2025

North American Rescue JETT Emergency Tool Recall: Structural Defect Risk

North American Rescue recalls JETT emergency tools due to potential structural defects that could compromise performance during use. Affected kits include TCCC Training Complete and other emergency response kits.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2637-2025Medical deviceNorth American Rescue ›
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Contact the company

Recalling firmNorth American Rescue LLC.35 Tedwall Ct · Greer, SC 29650-4791
✎ GovInfoNow plain-language explainer

North American Rescue is recalling JETT emergency tools that may have structural defects, risking failure during critical blood flow procedures. This could lead to improper use in emergency situations where timely intervention is needed. Read more at govinfonow.com/recall/51919-north-american-rescue-jett-emergency-tool-recall-structural-defect-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/51919-north-american-rescue-jett-emergency-tool-recall-structural-defect-risk · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2637-2025

Cite this page

“North American Rescue JETT Emergency Tool Recall: Structural Defect Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51919-north-american-rescue-jett-emergency-tool-recall-structural-defect-risk. Based on FDA recall #Z-2637-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2637-2025%22&limit=1).

The FDA announced on July 1, 2025, that North American Rescue LLC. is recalling JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, due to a manufacturing defect that may compromise structural integrity and performance. The agency classified the recall as Class II.

How to tell if you have it

  • Brand: North American Rescue
  • Product: JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088
  • UPC: 00842209100002
  • Lot codes for JETT: 021224-1, 81722-1, 81722-2, 121323-1
  • Kits containing the component: KIT, TCCC Training- Complete (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 ONE SKILLS REFILL (REF: 85-1900)
  • Distribution: Worldwide, including US states SC, OK, ID, KY, VA, NV, IL, TX, CA, FL, LA, NY, ME, PA, AR, AZ, AL, DE, MA, MS, HI, WA, MI, GA, NJ, UT, MD, OR, NC and countries KOR, JPN, BWA, SAU, BEL

The hazard

The device is used for unilateral or bilateral occlusion of blood flow to the lower limbs. A potential manufacturing defect may compromise the structural integrity of the device and its performance during use.

Context

GovInfoNow's records show North American Rescue LLC. has four other recalls on record since September 27, 2016. Other recent recalls include a March 27, 2026 recall of AIDBAGs for blood glucose meter error code risk and an August 27, 2021 recall of 10 ga ARS Decompression Needles for incorrect instructions. Similar recent recalls of similar products include a December 17, 2025 recall of Aju Pharm Genesis Dual Thread Screw-In Anchors for anchor breakage risk and an October 30, 2025 recall of Olympus HX-400U-30 Ligating Devices for unintentional loop fixation risk.

How to tell if you have this one

Check for the JETT tool (REF: 30-0088) inside TCCC Training Complete kits (REF: 85-0550) or other specified emergency response kits. Look for the unique identifiers listed in the recall notice.

  • Brand
    North American Rescue
  • Product
    JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Tool Identification

    Verify the JETT tool's unique identifier (UDI) matches the listed numbers in the recall notice.

  2. Contact Manufacturer

    Reach out to North American Rescue for specific instructions on how to handle the recalled items.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 29 states.

Alaska: nationwideAKMaine: named in the noticeMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: named in the noticeWAIdaho: named in the noticeIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: named in the noticeILWisconsin: nationwideWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: named in the noticeMAOregon: named in the noticeORNevada: named in the noticeNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: nationwideOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: nationwideCTCalifornia: named in the noticeCAUtah: named in the noticeUTColorado: nationwideCONebraska: nationwideNEMissouri: nationwideMOKentucky: named in the noticeKYWest Virginia: nationwideWVVirginia: named in the noticeVAMaryland: named in the noticeMDDelaware: named in the noticeDEArizona: named in the noticeAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: named in the noticeARTennessee: nationwideTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: nationwideDCOklahoma: named in the noticeOKLouisiana: named in the noticeLAMississippi: named in the noticeMSAlabama: named in the noticeALGeorgia: named in the noticeGAHawaii: named in the noticeHITexas: named in the noticeTXFlorida: named in the noticeFL

FDA distribution: “Worldwide - US Nationwide distribution in the states of SC, OK, ID, KY, VA, NV, IL, TX, CA, FL, LA, NY, LA, ME, PA, AR, AZ, AL, DE, MA, MS, HI, WA, MI, GA, NJ, UT, MD, OR, NC, NC, AL and the countries of KOR, JPN, BWA, SAU, BEL.” States read from FDA’s own wording; “not listed” means the notice does not name it.

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

Recall timeline

FDA published this recall 3 months after the firm started it.

1. Firm started the recall: Jul 1, 202512. FDA classified it Class II: Sep 26, 202523. Published in FDA’s Enforcement Report: Oct 8, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Other North American Rescue recalls

North American Rescue LLC. recalls AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits
March 27, 2026

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-2637-2025 (July 1, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2637-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA