Device recall
Z-0198-2016: Antibacterial Hydro Personal Catheter, Male 12 Fr, Product Code 63512, sold in…
FDA device recall · Class III · C.R. Bard, Inc.
Key facts
| Recall number (Z-number) | Z-0198-2016 |
|---|---|
| Recall event | 72398 |
| Product | Antibacterial Hydro Personal Catheter, Male 12 Fr, Product Code 63512, sold in boxes of 30 units |
| Product code | MJC |
| Recalling firm | C.R. Bard, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 1, 2016 |
| 510(k) numbers | K033477 |
| FEI number | 1018233 |
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