Device recall
Z-0189-04: Ross 22 FR Gastrostomy Tube, Item #156.
FDA device recall · Class II · Ross Products Division, Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-0189-04 |
|---|---|
| Recall event | 27691 |
| Product | Ross 22 FR Gastrostomy Tube, Item #156. |
| Product code | KNT |
| Recalling firm | Ross Products Division, Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 24, 2008 |
| 510(k) numbers | K861323 |
| FEI number | 1000136098 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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