Device recall
Z-3302-2024: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti-Reflux Valve, 12…
FDA device recall · Class II · Cardinal Health 200, LLC
Key facts
| Recall number (Z-number) | Z-3302-2024 |
|---|---|
| Recall event | 95214 |
| Product | (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti-Reflux Valve, 12 Fr/Ch (4.0 mm) x 48 in. (122 cm), Model #8888266114, Sterile; (b) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti-Reflux Valve, 14 Fr/Ch (4.7 mm) x 48 in. (122 cm), Model #8888266122, Sterile; (c)… |
| Product code | FEG |
| Recalling firm | Cardinal Health 200, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K880850 |
| FEI number | 3001236905 |
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