Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-3052-2020 — 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 (

U.S. FDA — Device Enforcement · Italy · 2020-09-08 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-3052-2020
Date of alert: 2020-09-08
Country / jurisdiction: Italy
Risk level: Class II
Risk type: recall
Brand: ESAOTE S.P.A
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 151004300

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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