Data Foundry

Medical device recalls 2020

AC/DC POWER SUPPLY for 7400 — Class II medical device recall Z-3052-2020

Terminated recall by ESAOTE S.P.A, reported 2020-10-07, distributed nationwide. The AC/DC adapter (power supply) of the portable ultrasound systems listed below that may result in the connec

Recall numberZ-3052-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmESAOTE S.P.A, Genova, N/A, Italy
Recall initiated2020-09-08
Classified2020-09-30
Reported by FDA2020-10-07
Terminated2023-04-17
DistributedNationwide (US)
Quantity989 adapters
Model numbers151004300, AHM180PS19-XE0338

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3052-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.