H&H Emergency Cricothyrotomy Kit — Class I medical device recall Z-0006-2014
Terminated recall by H & H Associates, reported 2013-10-09, distributed nationwide. Medical device tubing used for endotracheal airway application may become weakened and rendered ineffective.
| Recall number | Z-0006-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | H & H Associates, Ordinary, VA, United States |
| Recall initiated | 2013-08-27 |
| Classified | 2013-10-01 |
| Reported by FDA | 2013-10-09 |
| Terminated | 2015-01-13 |
| Distributed | Nationwide (US) |
| Quantity | 6,619 kits |
| Lot numbers | CKBD033, CKBD034, CKBE033, CKBF034, CKBG034, CKBP045, CKBP047, CKBQ047, CKBR060, CKBT065, CKBV070, CKBW070, CKBX070, CKBX071, CKBX076, CKBX078, CKBX079, CKBY079, CKBY080, CKBZ080, CKCA080 |
| Model numbers | 6515-01-573-0692, HHECT01, HHECTK01 |
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 for recall
Medical device tubing used for endotracheal airway application may become weakened and rendered ineffective.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0006-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.