Device recall
Z-0006-2014: H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN…
FDA device recall · Class I · H & H Associates
Key facts
| Recall number (Z-number) | Z-0006-2014 |
|---|---|
| Recall event | 66128 |
| 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. |
| Product code | BSK |
| Recalling firm | H & H Associates |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 13, 2015 |
| FEI number | 3003339833 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database