Device recall
Z-0449-03: Y-Type Blood/Solution Set, catalog #1C8117; Standard Blood Filter (170 to 260…
FDA device recall · Class II · Baxter Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-0449-03 |
|---|---|
| Recall event | 25247 |
| Product | Y-Type Blood/Solution Set, catalog #1C8117; Standard Blood Filter (170 to 260 micron), Drip Chamber Pump, Injection Site, Male Luer Lock Adapter, 88'' long, 10 drops per mL; Baxter Healthcare Corporation, Deerfield, IL 60015 |
| Product code | KSB |
| Recalling firm | Baxter Healthcare Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 30, 2003 |
| 510(k) numbers | K881321 |
| FEI number | 1416980 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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