Device recall
Z-0476-2016: Dressol-X, Radiopaque D-502, NDC 11004-502-40, Dental Use Only, Active…
FDA device recall · Class II · Rainbow Specialty & Health Products
Key facts
| Recall number (Z-number) | Z-0476-2016 |
|---|---|
| Recall event | 72726 |
| Product | Dressol-X, Radiopaque D-502, NDC 11004-502-40, Dental Use Only, Active Ingredients: A.S.A. (Acetylsalicylic Acid) + Eugenol |
| Product code | GDY |
| Recalling firm | Rainbow Specialty & Health Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2016 |
| FEI number | 3002654714 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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