Transducer C5-1 989605412042Recalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

11 FDA recall records name this device's identifier, 11 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, 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 3, 2025Class IIIOpen, Classified

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

   Z-2372-2025 · 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-2347-2025 · Root cause: Device Design · Recall details · FDA record ↗

3. Jul 3, 2025Class IIIOpen, Classified

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

   Z-2352-2025 · Root cause: Device Design · Recall details · FDA record ↗

4. Jul 3, 2025Class IIIOpen, Classified

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

   Z-2364-2025 · Root cause: Device Design · Recall details · FDA record ↗

5. Jul 3, 2025Class IIIOpen, Classified

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

   Z-2393-2025 · Root cause: Device Design · Recall details · FDA record ↗

6. Jul 3, 2025Class IIIOpen, Classified

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

   Z-2377-2025 · Root cause: Device Design · Recall details · FDA record ↗

7. Jul 3, 2025Class IIIOpen, Classified

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

   Z-2360-2025 · Root cause: Device Design · Recall details · FDA record ↗

8. Jul 3, 2025Class IIIOpen, Classified

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

   Z-2376-2025 · Root cause: Device Design · Recall details · FDA record ↗

9. Jul 3, 2025Class IIIOpen, Classified

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

   Z-2409-2025 · Root cause: Device Design · Recall details · FDA record ↗

10. Jul 3, 2025Class IIIOpen, Classified

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

    Z-2373-2025 · Root cause: Device Design · Recall details · FDA record ↗

11. May 28, 2025Class IIOpen, Classified

    Ultrasound transducer devices were refurbished beyond their useful life.

    Z-2049-2025 · Root cause: Process control · Recall details · FDA record ↗