Device recall
Z-0518-2014: Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR…
FDA device recall · Class II · Kimberly-Clark Corporation
Key facts
| Recall number (Z-number) | Z-0518-2014 |
|---|---|
| Recall event | 66859 |
| Product | Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usage: The device is designed to provide regional anesthesia. The device may contain syringes, needles and drugs |
| Product code | CAZ |
| Recalling firm | Kimberly-Clark Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 25, 2017 |
| 510(k) numbers | K941153 |
| FEI number | 1000015879 |
At a glance
- 1–9 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