Device recall
Z-0781-2023: VERIFY Steam Test Pack (20 Tests and 20 controls) Item Number: S3069 Intended…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-0781-2023 |
|---|---|
| Recall event | 91315 |
| Product | VERIFY Steam Test Pack (20 Tests and 20 controls) Item Number: S3069 Intended for use in installation testing and routine monitoring of steam and ethylene oxide sterilization processes |
| Product code | FRC |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K083665 |
| FEI number | 1527821 |
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