Device recall
Z-0724-2017: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile), Product…
FDA device recall · Class II · Halyard Health, Inc
Key facts
| Recall number (Z-number) | Z-0724-2017 |
|---|---|
| Recall event | 75683 |
| Product | Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile), Product Code 44965 NS; C-Section Drape with Clear Screen and Full Incise (Sterile), Product Code 44966 00; C-Section Drape with Clear Screen (Non-Sterile), Product Code 44967 NS; C-Section Drape with Clear Screen (Sterile)… |
| Product code | KKX |
| Recalling firm | Halyard Health, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 22, 2017 |
| 510(k) numbers | K862801 |
| FEI number | 3011270181 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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