FDAJuly 1, 2025device

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...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

north american rescuenorthnorth american

UPCs

0084220910000200842209110711850550091824850550090424850550030725850550052925850550052325850550082324850550080624850550062624850550052124850550111424

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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