Device recall
Z-0381-04: Kendall Kerlix Large Roll, 4.5 in X 4.1 yd, Sterile Product Number: 6730
FDA device recall · Class II · Kendall Healthcare Products Co
Key facts
| Recall number (Z-number) | Z-0381-04 |
|---|---|
| Recall event | 28090 |
| Product | Kendall Kerlix Large Roll, 4.5 in X 4.1 yd, Sterile Product Number: 6730 |
| Product code | NAD |
| Recalling firm | Kendall Healthcare Products Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2012 |
| FEI number | 1282497 |
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