Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01 Recalled by H & H Associates Due to Medical device tubing used for endotracheal airway application...
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 H & H Associates directly.
Affected Products
H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 mil poly bags, labeled in part ***H & H Associates, Inc. CAGE 1NNH6 www.gohandh.com Ordinary, VA 23131 (800) 326-5708***. The product is used to maintain fracture alignment.
Quantity: 6,619 kits
Why Was This Recalled?
Medical device tubing used for endotracheal airway application may become weakened and rendered ineffective.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About H & H Associates
H & H Associates has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report