Device recall
Z-1154-03: Interlink System Vented Nitroglycerin Set, 104 '', PVC Tubing Segment, Injection…
FDA device recall · Class II · Baxter Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-1154-03 |
|---|---|
| Recall event | 26772 |
| Product | Interlink System Vented Nitroglycerin Set, 104 '', PVC Tubing Segment, Injection Site, Male Luer Lock Adapter, catalog 2C7551; Baxter Healthcare Corporation, Deerfield, IL 60015 USA |
| Product code | FPA |
| Recalling firm | Baxter Healthcare Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2004 |
| 510(k) numbers | K832885 |
| 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