Device recall
Z-0707-03: The device is Labeled as SMART Control TRANSHEPATIC BILIARY STENT REF (PRODUCT…
FDA device recall · Class II · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-0707-03 |
|---|---|
| Recall event | 25712 |
| Product | The device is Labeled as SMART Control TRANSHEPATIC BILIARY STENT REF (PRODUCT NUMBER LISTED), VARIOUS LABELED SIZES . and lot numbers. Product is packed in a Tyvek pouch and further packed into a shelf carton. Product Numbers: C06020SB, C06020MB, C06030SB, C06030MB, C06040SB, C06040MB, C06060SB… |
| Product code | FGE |
| Recalling firm | Cordis Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 8, 2010 |
| 510(k) numbers | K021898, K023217 |
| FEI number | 1016427 |
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