Device recall
Z-1089-2016: IMPAK ACRYLIC RESIN LIQUID FOR BOTH IMPAK & IMPAK-PF POWDERS 1 qt. size (946…
FDA device recall · Class II · CMP Industries, Llc
Key facts
| Recall number (Z-number) | Z-1089-2016 |
|---|---|
| Recall event | 71148 |
| Product | IMPAK ACRYLIC RESIN LIQUID FOR BOTH IMPAK & IMPAK-PF POWDERS 1 qt. size (946 cc), Part Number 3306, and 11 oz. size (325 cc), Part Number 3748. Indicated for relining a denture surface for repairing a fractured denture, or forming a new denture base. |
| Product code | EBI |
| Recalling firm | CMP Industries, Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2018 |
| 510(k) numbers | K033020 |
| FEI number | 1315551 |
At a glance
- 1–9 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