Device recall
Z-2422-2015: IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Suction Wand is a…
FDA device recall · Class II · International Biophysics Corp.
Key facts
| Recall number (Z-number) | Z-2422-2015 |
|---|---|
| Recall event | 71911 |
| Product | IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Suction Wand is a component of Blood Recovery System for use in open heart procedures, autologous blood recovery and blood suction. It is a disposable, single use component. |
| Product code | DTS |
| Recalling firm | International Biophysics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 1, 2016 |
| 510(k) numbers | K963756 |
| FEI number | 1000117854 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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