Device recall
Z-1235-2022: AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
FDA device recall · Class II · Northgate Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-1235-2022 |
|---|---|
| Recall event | 90095 |
| Product | AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe |
| Product code | FFK |
| Recalling firm | Northgate Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 8, 2022 |
| 510(k) numbers | K130368 |
| FEI number | 1450997 |
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