# FDA recall Z-1235-2022

> **Northgate Technologies, Inc.** · Class II · device recall initiated 2022-04-13.

## Product

AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe

## Reason for recall

Product labeled incorrectly.

## Distribution

US Nationwide distribution in the state of MA.

## Key facts

- **Recall number:** Z-1235-2022
- **Recalling firm:** Northgate Technologies, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-04-13
- **Report date:** 2022-06-15
- **Termination date:** 2022-11-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Elgin, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1235-2022

## Citation

> AI Analytics. FDA recall Z-1235-2022. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1235-2022. Source: US FDA. Licensed CC0.

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