Device recall
Z-2058-2017: Medi-Therm Hyper/Hypothermia System, MTA7900
FDA device recall · Class II · Stryker Medical Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2058-2017 |
|---|---|
| Recall event | 77014 |
| Product | Medi-Therm Hyper/Hypothermia System, MTA7900 |
| Product code | DWJ |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2017 |
| 510(k) numbers | K912051 |
| FEI number | 1831750 |
At a glance
- 1–9 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