Device recall
Z-1628-2009: Boston Scientific EndoVive 20Fr (6.7 mm) Safety PEG Kit, Push Method, for use…
FDA device recall · Class II · Boston Scientific Corp
Key facts
| Recall number (Z-number) | Z-1628-2009 |
|---|---|
| Recall event | 52189 |
| Product | Boston Scientific EndoVive 20Fr (6.7 mm) Safety PEG Kit, Push Method, for use with pre-filled lidocaine syringe, latex free, sterile, Boston Scientific Corp., Natick, MA; Cat. no./REF 6673, inner pouch UPN M00566730 and outer carton UPN M00566731. The devices are indicated for providing nutrition… |
| 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