# FDA recall Z-2276-2019

> **NeuroLogica Corporation** · Class II · device recall initiated 2019-07-25.

## Product

WS80A Diagnostic Ultrasound System Version 1.00.16, 3.00.17, 3.00.18, 3.00.19, 3.01.00, 3.01.01, 3.01.02, 3.01.03, 3.01.04, 3.01.05, 3.01.06, 3.01.07,  3.01.08, 3.01.09, 4.00.08, 4.00.09, 4.00.10, 4.00.11, 4.01.00, 4.01.01, 4.01.02,  4.01.03, 4.01.04, 4.01.05, 4.01.06, 4.01.07, 4.01.08, 4.01.09.

## Reason for recall

There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.

## Distribution

US Nationwide

## Key facts

- **Recall number:** Z-2276-2019
- **Recalling firm:** NeuroLogica Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-25
- **Report date:** 2019-08-21
- **Termination date:** 2020-09-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Danvers, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2276-2019

## Citation

> AI Analytics. FDA recall Z-2276-2019. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-2276-2019. Source: US FDA. Licensed CC0.

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