Device recall
Z-0836-2018: STRYKER CASSETTE PUMP, AHTO Tube Set, labeled sterile. Includes the following…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0836-2018 |
|---|---|
| Recall event | 78668 |
| Product | STRYKER CASSETTE PUMP, AHTO Tube Set, labeled sterile. Includes the following: a. Stryker AHTO Tube Set Packaging (Model 0250070600); b. Stryker AHTO Tube Set with Tip Packaging (Model 0250070620); |
| Product code | GCX |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2024 |
| 510(k) numbers | K042454 |
| 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