Device recall
Z-1133-2012: BardPort M.R.I. Implanted Port with Attachable 6 Fr. ChronoFlex Open-Ended…
FDA device recall · Class III · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-1133-2012 |
|---|---|
| Recall event | 61185 |
| Product | BardPort M.R.I. Implanted Port with Attachable 6 Fr. ChronoFlex Open-Ended Single-Lumen Venous Catheter and Peel-Apart Introducer Kit. Subcutaneous implanted intravascular infusion port and catheter is used to provide repeated access to the vascular system for the delivery of medications… |
| Product code | LJT |
| Recalling firm | Bard Access Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 30, 2012 |
| 510(k) numbers | K873213 |
| 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