Class II — Northgate Technologies, Inc.
| Recalling firm | Northgate Technologies, Inc. |
|---|---|
| Registered facility | Northgate Technologies Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Product labeled incorrectly. |
| Product | AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe |
| Quantity | 55 probes |
| Distribution | US Nationwide distribution in the state of MA. |
| Initiated | 2022-04-13 |
| Classified | 2022-06-03 |
| Terminated | 2022-11-08 |
| Recall number | Z-1235-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Northgate Technologies, Inc. (Z-1235-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90095/
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