H & H Associates recalls H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 m

Recalled October 9, 2013 · FDA recall Z-0006-2014 · H & H Associates

Hazard

Medical device tubing used for endotracheal airway application may become weakened and rendered ineffective. · FDA Class I

Units

6,619 kits

Sold at

Nationwide distribution.

Description

Medical device tubing used for endotracheal airway application may become weakened and rendered ineffective.

Product

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.

Manufacturer(s)

H & H Associates

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →