Device recall
Z-2291-2019: MICRO-TEMP LT System, Model 749- Localized Heat Therapy System is intended to…
FDA device recall · Class III · Cincinnati Sub-Zero Products LLC, a Gentherm Company
Key facts
| Recall number (Z-number) | Z-2291-2019 |
|---|---|
| Recall event | 83387 |
| Product | MICRO-TEMP LT System, Model 749- Localized Heat Therapy System is intended to warm a patient's body part through conductive heat transfer. |
| Product code | ILO |
| Recalling firm | Cincinnati Sub-Zero Products LLC, a Gentherm Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 13, 2020 |
| 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