Device recall
Z-1525-2010: PowerPort isp M.R.I Implanted Port without Suture Plugs with attachable 6F…
FDA device recall · Class II · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-1525-2010 |
|---|---|
| Recall event | 55175 |
| Product | PowerPort isp M.R.I Implanted Port without Suture Plugs with attachable 6F Chronoflex Polyurethane Open-ended Single -Lumen Venous Catheter, BARD Access Systems Assembled in Mexico Indicated for patient therapies requiring repeated access to the vascular system for the infusion of medications, I.V… |
| Product code | LJT |
| Recalling firm | Bard Access Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 1, 2010 |
| 510(k) numbers | K072549 |
| FEI number | 3006260740 |
At a glance
- 1–9 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