Device recall
Z-0864-06: Kimberly Clark * 20' Minibore Extension Line * Single Use * Sterile * Rx only *…
FDA device recall · Class II · Kimberly-Clark Corporation
Key facts
| Recall number (Z-number) | Z-0864-06 |
|---|---|
| Recall event | 35158 |
| Product | Kimberly Clark * 20' Minibore Extension Line * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA. This is a Pain Management Product that is sold in a wide variety… |
| Product code | FPK |
| Recalling firm | Kimberly-Clark Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 10, 2011 |
| 510(k) numbers | K935642 |
| FEI number | 1000015879 |
At a glance
- 1–9 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