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Transducer S7-3tRecalls & reported problems across all models

Philips Ultrasound LLC · 2 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

5 open recalls name at least one Transducer S7-3t model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
22
Deaths reported
1
Injuries reported
5
Recalls
5

We found 2 models of Transducer S7-3t by Philips Ultrasound LLC in the FDA's device registry (GUDID). Together they are named in 22 adverse event reports in the FDA's MAUDE database, received between Aug 3, 2017 and Jan 19, 2021 — classified as 1 death, 5 injuries, 16 malfunctions.

The most frequently reported specific device problem is “Temperature Problem” (4 reports).

5 FDA recall records name at least one of these models by its device identifier, 5 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Transducer S7-3t recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Jul 3, 2025Class IIIOpen, Classified

    To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

    Z-2412-2025 · Root cause: Device Design · Recall details · FDA record ↗

  2. Jul 3, 2025Class IIIOpen, Classified

    To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

    Z-2395-2025 · Root cause: Device Design · names 2 of these models · Recall details · FDA record ↗

  3. May 28, 2025Class IIOpen, Classified

    Ultrasound transducer devices were refurbished beyond their useful life.

    Z-2067-2025 · Root cause: Process control · Recall details · FDA record ↗

  4. May 28, 2025Class IIOpen, Classified

    Ultrasound transducer devices were refurbished beyond their useful life.

    Z-2061-2025 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗

  5. May 28, 2025Class IIOpen, Classified

    Ultrasound transducer devices were refurbished beyond their useful life.

    Z-2060-2025 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗

Most reported Transducer S7-3t problems

Device problems

  • Adverse Event Without Identified Device or Use Problem5
  • Temperature Problem4
  • Positioning Problem3
  • Crack2
  • Display or Visual Feedback Problem2
  • Mechanical Jam2
  • Activation Problem1
  • Defective Device1

Patient problems

  • No Consequences Or Impact To Patient6
  • No Known Impact Or Consequence To Patient6
  • Burn, Thermal5
  • No Patient Involvement4
  • Death1
  • No Clinical Signs, Symptoms or Conditions1
  • Perforation of Esophagus1

Transducer S7-3t models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

Recent Transducer S7-3t adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Philips Ultrasound LLC products

All Philips Ultrasound LLC devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page