Device recall
Z-0263-2008: Baxter Duploject Easy Prep, Fibrin Sealant Preparation and Application System…
FDA device recall · Class II · Baxter Bioscience
Key facts
| Recall number (Z-number) | Z-0263-2008 |
|---|---|
| Recall event | 45489 |
| Product | Baxter Duploject Easy Prep, Fibrin Sealant Preparation and Application System ISO; Product Codes: 1500949, 1500950, 1500951, 1501250 & 1501252, Baxter Healthcare Corporation, Deerfield, IL 60015 |
| Product code | FMF |
| Recalling firm | Baxter Bioscience |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2009 |
| 510(k) numbers | K020666 |
| FEI number | 1417572 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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