Device recall
Z-1788-2014: Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number…
FDA device recall · Class II · Kerr Corporation
Key facts
| Recall number (Z-number) | Z-1788-2014 |
|---|---|
| Recall event | 68426 |
| Product | Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device is to be used as a dental restorative material in the treatment of dental caries. |
| Product code | EJJ |
| Recalling firm | Kerr Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 27, 2014 |
| 510(k) numbers | K951663 |
| FEI number | 1815757 |
At a glance
- 1–9 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