Device recall
Z-0782-2017: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including…
FDA device recall · Class II · Ultroid Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0782-2017 |
|---|---|
| Recall event | 75055 |
| Product | Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes |
| Product code | KNS |
| Recalling firm | Ultroid Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 11, 2019 |
| 510(k) numbers | K023706, K030315 |
| FEI number | 3013037032 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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