Device recall
Z-1728-2019: Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-690…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1728-2019 |
|---|---|
| Recall event | 82489 |
| Product | Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-690, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile. |
| Product code | HIF |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2024 |
| 510(k) numbers | K003792 |
| FEI number | 2936485 |
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