Device recall
Z-1242-06: Kimberly-Clark/Ballard medical R2 triangle shaped non-radiolucent multifunction…
FDA device recall · Class II · Kimberly-Clark Corporation
Key facts
| Recall number (Z-number) | Z-1242-06 |
|---|---|
| Recall event | 35559 |
| Product | Kimberly-Clark/Ballard medical R2 triangle shaped non-radiolucent multifunction electrode products for adults. |
| Product code | MKJ |
| Recalling firm | Kimberly-Clark Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 14, 2007 |
| 510(k) numbers | K935371 |
| 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