# FDA recall Z-2275-2019

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

## Product

HS70A Diagnostic Ultrasound System Version 2.01.00, 2.01.01, 2.01.02, 2.01.03, 2.01.04, 2.01.05, 2.01.06, 1.00.06, 1.00.07, 1.00.08, 1.00.09, 1.00.10, 1.00.11, 1.00.12

## 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-2275-2019
- **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-2275-2019

## Citation

> AI Analytics. FDA recall Z-2275-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2275-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*