Device recall
Z-2836-2011: Kimberly-Clark, Three Quarter Drape, Non sterile/Disposable, Surgical drape.
FDA device recall · Class II · Kimberly-Clark Corporation
Key facts
| Recall number (Z-number) | Z-2836-2011 |
|---|---|
| Recall event | 59161 |
| Product | Kimberly-Clark, Three Quarter Drape, Non sterile/Disposable, Surgical drape. |
| Product code | KKX |
| Recalling firm | Kimberly-Clark Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 14, 2011 |
| FEI number | 1000015879 |
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