Device recall
Z-0518-03: Baxter Interlink System Microbore T-Connector Extension Set with 0.22 Micron…
FDA device recall · Class I · Baxter Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-0518-03 |
|---|---|
| Recall event | 25088 |
| Product | Baxter Interlink System Microbore T-Connector Extension Set with 0.22 Micron High Pressure Pediatric Filter, catalog 2N3333; Baxter Healthcare Corporation, Deerfield, IL 60015; 200 units per case |
| Product code | FPA |
| Recalling firm | Baxter Healthcare Corp. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Feb 4, 2004 |
| 510(k) numbers | K791496, K921899, K925126 |
| FEI number | 1416980 |
At a glance
- 1–9 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