Device recall
Z-1743-2017: Covidien Kerlix Super Sponge Saline Dressing, Sterile Item Code: 3338 Curity…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-1743-2017 |
|---|---|
| Recall event | 76606 |
| Product | Covidien Kerlix Super Sponge Saline Dressing, Sterile Item Code: 3338 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help promote biological cleansing within the wound and aid in the autolytic debridement process. |
| Product code | NAD |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2019 |
| FEI number | 1219930 |
At a glance
- None 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