Device recall
Z-1048-05: Baxter Interlink System Huber Needle Extension Set; a sterile 10'' fluid pathway…
FDA device recall · Class III · Baxter Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-1048-05 |
|---|---|
| Recall event | 32191 |
| Product | Baxter Interlink System Huber Needle Extension Set; a sterile 10'' fluid pathway with an Interlink Y-Injection Site and 3/4'' x 22 gauge needle; Manufactured for Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A.; product code 2N3709 |
| Product code | FPA |
| Recalling firm | Baxter Healthcare Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 23, 2006 |
| 510(k) numbers | K961495 |
| FEI number | 1416980 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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