Device recall
Z-0657-06: Baxter Minivolume Extension Set, product code JC9944; An Rx sterile…
FDA device recall · Class II · Baxter Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-0657-06 |
|---|---|
| Recall event | 34290 |
| Product | Baxter Minivolume Extension Set, product code JC9944; An Rx sterile, nonpyrogenic fluid pathway, 8'', 0.4 mL Vol., with Luer Activated Valve; Baxter Corporation, Toronto, Ontario, Canada; Made in Canada |
| Product code | FPA |
| Recalling firm | Baxter Healthcare Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 18, 2008 |
| FEI number | 1416980 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 1,000+ 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