# FDA recall Z-3052-2020

> **ESAOTE S.P.A** · Class II · device recall initiated 2020-09-08.

## Product

AC/DC POWER SUPPLY for 7400, Part Number 151004300, XP Power Model Number AHM180PS19-XE0338, AC/DC Adapter associated with the following portable ultrasound diagnostic systems: The AC/DC adapter is intended for use with the following portable ultrasound systems:  MyLabAlpha	(101740000)  MyLabGamma	(101741000)  MyLabOmega	(101740004)  MyLabSigma	(101741004)  MyLabSigma elite	(101741007)  MyLabAlphaVET	(101740001)  MyLabGammaVET	(101741001)  MyLabDelta	(100743000)  MyLabDeltaVET	(100743001)  MyLabOmegaVET	(101740005)  MyLabSigmaVET	(101741005)

## Reason for recall

The AC/DC adapter (power supply) of the portable ultrasound systems listed below that may result in the connector heating up, generating smoke and melting.    This condition is caused by the mechanical stress of the connection between the AC/DC power adapter and the mains cable over the time of use.

## Distribution

US Nationwide

## Key facts

- **Recall number:** Z-3052-2020
- **Recalling firm:** ESAOTE S.P.A
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-08
- **Report date:** 2020-10-07
- **Termination date:** 2023-04-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Genova, N/A, Italy

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3052-2020

## Citation

> AI Analytics. FDA recall Z-3052-2020. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-3052-2020. Source: US FDA. Licensed CC0.

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