Device recall
Z-0040-06: Enteryx Procedure Kit Order No.: M00572600 -US and M00572500 -OUS
FDA device recall · Class I · Boston Scientific Corporation
Key facts
| Recall number (Z-number) | Z-0040-06 |
|---|---|
| Recall event | 33529 |
| Product | Enteryx Procedure Kit Order No.: M00572600 -US and M00572500 -OUS |
| Product code | LNM |
| Recalling firm | Boston Scientific Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 24, 2006 |
| 510(k) numbers | K042882 |
| FEI number | 3001451463 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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