# FDA recall Z-0073-2018

> **Northgate Technologies, Inc.** · Class II · device recall initiated 2017-05-24.

## Product

Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Autolith lithotripter. electrohydraulic lithotripsy (EHL) is a method that allows large stones to be fragmented and removed percutaneously or endoscopically.

## Reason for recall

The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the probe will not allow the mislabeled product to be used with the incorrect generator. Could Delay Care.

## Distribution

US Distribution to the following states :  MA, NE and  TN  and Internationally  to Canada.

## Key facts

- **Recall number:** Z-0073-2018
- **Recalling firm:** Northgate Technologies, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-24
- **Report date:** 2017-11-15
- **Termination date:** 2020-06-09

- **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-0073-2018

## Citation

> AI Analytics. FDA recall Z-0073-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0073-2018. Source: US FDA. Licensed CC0.

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