Device recall
Z-3173-2011: BardPort Titanium Implanted Port. Bard Access Systems. Assembled in Mexico. A…
FDA device recall · Class III · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-3173-2011 |
|---|---|
| Recall event | 59830 |
| Product | BardPort Titanium Implanted Port. Bard Access Systems. Assembled in Mexico. A totally implantable vascular access device designed to provide long term repeated access to the vascular system |
| Recalling firm | Bard Access Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 30, 2012 |
| 510(k) numbers | K050310 |
| FEI number | 3006260740 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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