Device recall
Z-0361-05: AMPLATZER Delivery System 180-degree curve, order no. 9-DEL-8F-180/80. Product…
FDA device recall · Class II · AGA Medical Corporation
Key facts
| Recall number (Z-number) | Z-0361-05 |
|---|---|
| Recall event | 30481 |
| Product | AMPLATZER Delivery System 180-degree curve, order no. 9-DEL-8F-180/80. Product is labeled as Sterile EO. Amplatzer Occluder Device and Delivery System is comprised of delivery sheath, delivery cable, dilator, loading device and pin vise. The Delivery and Exchange Systems are placed onto polyboard… |
| Product code | GBK |
| Recalling firm | AGA Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 26, 2006 |
| FEI number | 3005334138 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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