Device recall
Z-2423-2015: IBC Aortic Punch Catalog Numbers APM40, APL48A, APM44A, APL40A, APM40A, CVAPL36…
FDA device recall · Class II · International Biophysics Corp.
Key facts
| Recall number (Z-number) | Z-2423-2015 |
|---|---|
| Recall event | 71911 |
| Product | IBC Aortic Punch Catalog Numbers APM40, APL48A, APM44A, APL40A, APM40A, CVAPL36, CVAPL40, CVAPL44, CVAPL48, CVAPL52, APM28BM, APM36BM, APM40BM, APM44BM, APM48BM, APM40BK, APM48BK, APM36BK, APM44BK, APM28, APM36, APL44, APM40 Product Usage: The IBC Aortic Punch is a single-use, disposable surgical… |
| Product code | DWS |
| Recalling firm | International Biophysics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 1, 2016 |
| FEI number | 1000117854 |
At a glance
- None 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