Device recall
Z-0349-2017: Model 055: Thermophore Classic, Professional Quality, Deep-Heat Therapy, Model…
FDA device recall · Class II · Battle Creek Equipment Co.
Key facts
| Recall number (Z-number) | Z-0349-2017 |
|---|---|
| Recall event | 73286 |
| Product | Model 055: Thermophore Classic, Professional Quality, Deep-Heat Therapy, Model 055 Large 14' x 27", Model 056: Thermophore Classic, Professional Quality Deep-Heat Therapy, Model 056 Medium 14" x 14", Model 077: Thermophore Classic Professional Quality Deep-Heat Therapy, Model 077 Petite 4"x… |
| Product code | IRT |
| Recalling firm | Battle Creek Equipment Co. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 11, 2018 |
| FEI number | 1833125 |
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