Device recall
Z-1203-2016: Covidien Dover KIT/STERILE PRESERVE CULT Item Code: 8000SA Castile soap…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-1203-2016 |
|---|---|
| Recall event | 73121 |
| Product | Covidien Dover KIT/STERILE PRESERVE CULT Item Code: 8000SA Castile soap towelettes are used to clean the genital area for male and female patients |
| Product code | KOY |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 20, 2017 |
| 510(k) numbers | K030813 |
| FEI number | 1219930 |
At a glance
- 1–9 Linked 510(k)s
- 100–999 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