Device recall
Z-3016-2020: KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal…
FDA device recall · Class II · Cardinal Health 200, LLC
Key facts
| Recall number (Z-number) | Z-3016-2020 |
|---|---|
| Recall event | 86178 |
| Product | KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus. |
| Product code | LRP |
| Recalling firm | Cardinal Health 200, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2021 |
| FEI number | 3002973487 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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