Device recall
Z-0902-2007: Surge Medical Solutions brand 15 Fr. (5.0mm) Retrograde Cardioplegia Cannula…
FDA device recall · Class II · Surge Medical Solutions, LLC
Key facts
| Recall number (Z-number) | Z-0902-2007 |
|---|---|
| Recall event | 37806 |
| Product | Surge Medical Solutions brand 15 Fr. (5.0mm) Retrograde Cardioplegia Cannula, self-inflating balloon 18 mm, rigid insertion stylet, sterile, REF CODE: RSR-M014S. |
| Product code | DWF |
| Recalling firm | Surge Medical Solutions, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 10, 2009 |
| 510(k) numbers | K964393 |
| FEI number | 3003964340 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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