Device recall
Z-0496-2022: Electri-Cool II Portable Cold Therapy Unit, Model Number 767, Part Number 86193
FDA device recall · Class II · Gentherm Medical, LLC
Key facts
| Recall number (Z-number) | Z-0496-2022 |
|---|---|
| Recall event | 89193 |
| Product | Electri-Cool II Portable Cold Therapy Unit, Model Number 767, Part Number 86193 |
| Product code | ILO |
| Recalling firm | Gentherm Medical, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2023 |
| FEI number | 1516825 |
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