Device recall
Z-0908-2014: Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators…
FDA device recall · Class II · Medtronic Cardiovascular Surgery-the Heart Valve Division
Key facts
| Recall number (Z-number) | Z-0908-2014 |
|---|---|
| Recall event | 67242 |
| Product | Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators are used with the Mosaic Porcine Aortic Bioprostheses. |
| Product code | LWR |
| Recalling firm | Medtronic Cardiovascular Surgery-the Heart Valve Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 30, 2014 |
| FEI number | 2025587 |
At a glance
- None 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