EPIQ 7 Ultrasound System 795200Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884838107441), received between Jun 3, 2026 and Jun 3, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Battery Problem” (1 report).

1 FDA recall record name this device's identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Jul 14, 2022Class IICompleted

   Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.

   Z-1007-2026 · Root cause: Software Design Change · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 3, 2026Battery Problem

  IT WAS REPORTED EPIQ 7G ULTRASOUND SYSTEM'S UNINTERRUPTIBLE POWER SUPPLY (UPS) HAD AN ODOR AND ELECTROLYTE-LIQUID LEAKAGE. THE FAILURE OCCURRED OUTSIDE OF CLINICAL USE AND NO PATIENT OR USER HARM ASSOCIATED WITH THE EVENT. THE SERVICE ENGINEER DETERMINED THE LIKELY CAUSE OF THE LEAKAGE WAS FROM THE BATTERY. THE EXTERNAL UPS WAS REPLACED TO ADDRESS THE CUSTOMER'S IMMEDIATE CONCERNS. PHILIPS HAS STARTED AN INVESTIGATION, AND UPON COMPLETION, A FOLLOW UP REPORT WILL BE SUBMITTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25373831 ↗