Device recall
Z-1631-2009: Boston Scientific EndoVive 24F (8 mm) Standard PEG Kit, Push Method, latex free…
FDA device recall · Class II · Boston Scientific Corp
Key facts
| Recall number (Z-number) | Z-1631-2009 |
|---|---|
| Recall event | 52189 |
| Product | Boston Scientific EndoVive 24F (8 mm) Standard PEG Kit, Push Method, latex free, sterile, Boston Scientific Corp., Natick, MA; inner pouch UPN M00568250 and outer carton UPN M00568251. The devices are indicated for providing nutrition directly into the stomach in adult and pediatric patients who are… |
| Product code | KNT |
| Recalling firm | Boston Scientific Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2010 |
| 510(k) numbers | K031538 |
| FEI number | 1828132 |
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