Device recall
Z-1736-2022: Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam…
FDA device recall · Class III · Steris Corporation Hopkins Facility
Key facts
| Recall number (Z-number) | Z-1736-2022 |
|---|---|
| Recall event | 90763 |
| Product | Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design. |
| Product code | JOJ |
| Recalling firm | Steris Corporation Hopkins Facility |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 30, 2024 |
| 510(k) numbers | K162758 |
| FEI number | 3000251274 |
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