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SONNET Control Unit black 30750Recalls & reported problems

Med-El Elektromedizinische Geräte Gesellschaft m.b.H. · Audio Processor · Class 3

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

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 09008737307509), received between Feb 7, 2023 and Feb 7, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “No Device Output” (1 report).

4 other recalls cover devices cleared under the same FDA submission (P000025); they may or may not involve this specific model.

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.

Most reported problems

Device problems

  • No Device Output1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionFeb 7, 2023No Device Output; No Device Output

    A FINETUNER ECHO WAS RETURNED TO SERVICE AND REPAIR. UPON PRELIMINARY INVESTIGATION AT SERVICE AND REPAIR IT WAS DETERMINED THERE IS FAILURE OF THE TANTALUM CAPACITOR. ACCORDING TO THE REPAIR REQUEST FORM THE SCREEN WAS FROZEN AND RESETTING DID NOT RESOLVE THE ISSUE. THE DEVICE HAD BEEN IN USE SINCE (B)(6) 2022.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16310035 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P000025. One submission often covers many models, so check the product and lot details in each record.

  • Z-2356-2024 · Apr 18, 2024 · Open, Classified
    Mi1250 SYNCHRONY 2, Item Numbers: a) 39541, FLEXSOFT S-Vector; b) 39545, FLEX28 S-Vector; c) 39547, FLEX26 S-Vector; Cochlear Implant
  • Z-2138-2019 · Oct 16, 2018 · Terminated
    MED EL Cochlear Implant System, PULSARci100 Standard - Product Usage: The PULSARci100 Implant is an implantable part of the MED EL Cochlear Implant System and can only be used toge
  • Z-2136-2019 · Oct 16, 2018 · Terminated
    MED EL Cochlear Implant System, Mi1000 MED EL CONCERTO, sold under the following implant types: a. Mil000 CONCERTO PIN +FLEX28; b. Mi1000 CONCERTO +FLEX28; c. Mi100
  • Z-2137-2019 · Oct 16, 2018 · Terminated
    MED EL Cochlear Implant System, SONATATIi100, sold under the following implant types: a. SONATAti100 FLEXsoft; b. SONATAti100 H Standard; c. SONATAti100 Standard

Other IMPLANT, COCHLEAR devices

All IMPLANT, COCHLEAR devices →

Sources and updates

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