Device recall
Z-0421-05: Bosworth Superbite Zinc Oxide Eugenol Bite Registration Paste Kit; the kit…
FDA device recall · Class III · Harry J Bosworth Company
Key facts
| Recall number (Z-number) | Z-0421-05 |
|---|---|
| Recall event | 30743 |
| Product | Bosworth Superbite Zinc Oxide Eugenol Bite Registration Paste Kit; the kit consists of one 3.25 oz. tube of Accelerator - Blue, and one 7.5 oz. tube of Base - White, which are mixed as needed to make the registration paste; The Bosworth Company, 7227 North Hamlin Avenue, Skokie, IL 60076-3999… |
| Product code | ELW |
| Recalling firm | Harry J Bosworth Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 26, 2006 |
| FEI number | 1410638 |
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