Device recall
Z-0292-2019: IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1, Class I, 1 Quart (946ml)…
FDA device recall · Class II · CMP Industries, Llc
Key facts
| Recall number (Z-number) | Z-0292-2019 |
|---|---|
| Recall event | 81206 |
| Product | IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1, Class I, 1 Quart (946ml) REF:3306. Product Usage - Impak Elastic Acrylic Resin Liquid, Used for Dental Splints and Dental Nightguards |
| Product code | EBI |
| Recalling firm | CMP Industries, Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 19, 2020 |
| FEI number | 1315551 |
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