Device recall
Z-1969-2019: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity…
FDA device recall · Class II · Pharmaceutical Innovations, Inc.
Key facts
| Recall number (Z-number) | Z-1969-2019 |
|---|---|
| Recall event | 83213 |
| Product | ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution. |
| Product code | GYB |
| Recalling firm | Pharmaceutical Innovations, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 29, 2020 |
| FEI number | 2241583 |
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