Device recall
Z-0153-2016: OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization…
FDA device recall · Class II · Innovative Sterlization Technologies LLC
Key facts
| Recall number (Z-number) | Z-0153-2016 |
|---|---|
| Recall event | 72011 |
| Product | OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization container used to steam sterilize medical devices |
| Product code | KCT |
| Recalling firm | Innovative Sterlization Technologies LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2016 |
| 510(k) numbers | K052567 |
| FEI number | 3010772758 |
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