Device recall
Z-1013-2018: T/Pump temperature therapy pump, Models TP700 and TP700C
FDA device recall · Class III · Stryker Medical Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1013-2018 |
|---|---|
| Recall event | 79302 |
| Product | T/Pump temperature therapy pump, Models TP700 and TP700C |
| Product code | ILO |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 9, 2019 |
| 510(k) numbers | K073675 |
| 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