Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT) Recalled by North American Rescue LLC. Due to Device used for unilateral or bilateral occlusion of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact North American Rescue LLC. directly.
Affected Products
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 ONE SKILLS REFILL, REF: 85-1900
Quantity: 552
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About North American Rescue LLC.
North American Rescue LLC. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report