Device recall
Z-2191-2015: American Catheter / Cholangiogram Catheter 9100 Series.
FDA device recall · Class II · American Catheter Corp
Key facts
| Recall number (Z-number) | Z-2191-2015 |
|---|---|
| Recall event | 71263 |
| Product | American Catheter / Cholangiogram Catheter 9100 Series. |
| Product code | GBZ |
| Recalling firm | American Catheter Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 14, 2016 |
| FEI number | 1000151187 |
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