Device recall
Z-1300-2014: PowerPort Slim Implantable Port, indicated for patient therapies requiring…
FDA device recall · Class II · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-1300-2014 |
|---|---|
| Recall event | 67567 |
| Product | PowerPort Slim Implantable Port, indicated for patient therapies requiring repeated access to the vascular system. Product Codes: 1716000, 1716070 |
| Product code | LJT |
| Recalling firm | Bard Access Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 5, 2014 |
| FEI number | 3006260740 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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