Device recall
Z-1875-2008: VisuaLine Tricyclic Antidepressants: Six Dip (COC-THC-OPI-MET-BZD-OXD); Six Dip…
FDA device recall · Class II · Sun Biomedical Laboratories, Inc.
Key facts
| Recall number (Z-number) | Z-1875-2008 |
|---|---|
| Recall event | 48464 |
| Product | VisuaLine Tricyclic Antidepressants: Six Dip (COC-THC-OPI-MET-BZD-OXD); Six Dip (COC-THC-OPI-MET-PCP-OXD); Eight DIP (COC-THC-OPI-MET-AMP-BAR-BZD-OXD); Nine Dip (COC-THC-OPI-MET-PCP-AMP-BAR-BZD-TCA); Ten Dip X (COC-THC-OPI-MET-PCP-AMP-BAR-BZD-MTD-TCA); Ten Dip… |
| Product code | DJR |
| Recalling firm | Sun Biomedical Laboratories, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 10, 2009 |
| FEI number | 1000526795 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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