FDA Device recall Z-0006-2014
H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 mil poly bags, label…
- FDA Device
- Class I
- terminated
- Published 2013-10-09
On 2013-10-09 the FDA classified a Class I recall of H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 mil poly bags, label… by H And H Associates, citing medical device tubing used for endotracheal airway application may become weakened and rendered ineffective.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0006-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-08-27 |
| Published | 2013-10-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | H And H Associates |
| Distribution | US |
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.
Reason
Medical device tubing used for endotracheal airway application may become weakened and rendered ineffective.
Identifiers
| code_info | Lots\EXP Dates: CKBD033, CKBE033 August 2015 CKBD034, CKBF034, CKBG034 August 2015 CKBP045 November 2015 CKBP047,…Lots\EXP Dates: CKBD033, CKBE033 August 2015 CKBD034, CKBF034, CKBG034 August 2015 CKBP045 November 2015 CKBP047, CKBQ047 November 2015 CKBR060 February 2016 CKBT065 April 2016 CKBV070, CKBW070, CKBX070 May 2016 CKBX071 May 2016 CKBX076 June 2016 CKBX078 July 2016 CKBX079, CKBY079 July 2016 CKBY080, CKBZ080, CKCA080 July 2016. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0006-2014%22
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