Device recall
Z-0519-03: Baxter Microbore 3-Lead Extension Set with 0.22 Micron High Pressure Pediatric…
FDA device recall · Class I · Baxter Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-0519-03 |
|---|---|
| Recall event | 25088 |
| Product | Baxter Microbore 3-Lead Extension Set with 0.22 Micron High Pressure Pediatric Filter, catalog 2N3342; Baxter Healthcare Corporation, Deerfield, IL 60015; 50 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, K915390 |
| 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