Device recall
Z-1779-2019: Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product…
FDA device recall · Class II · Skytron, Div. The KMW Group, Inc
Key facts
| Recall number (Z-number) | Z-1779-2019 |
|---|---|
| Recall event | 82650 |
| Product | Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use in health care facilities. The Integrity Sterilizer incorporates high-pressure steam to sterilize nonporous or porous items and materials used in the health care… |
| Product code | FLE |
| Recalling firm | Skytron, Div. The KMW Group, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2020 |
| 510(k) numbers | K132439 |
| FEI number | 1825014 |
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