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Mi1200 SYNCHRONY PIN +FLEX26 36618Recalls & reported problems

Med-El Elektromedizinische Geräte Gesellschaft m.b.H. · Cochlear Implant · Class 3 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 09008737366186), received between Apr 17, 2023 and Jul 3, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Impedance Problem” (2 reports).

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 16, 2026.

Most reported problems

Device problems

  • Impedance Problem2

Patient problems

  • Failure of Implant2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 3, 2023Impedance Problem; Impedance Problem

    IN SITU MEASUREMENTS REPORTEDLY SHOWED AFFECTED CHANNELS. REIMPLANTATION IS SCHEDULED FOR (B)(6) 2023

    Patient problems: Failure of Implant

    MAUDE report 17246820 ↗
  • MalfunctionApr 17, 2023Impedance Problem; Impedance Problem

    THE USER'S HEARING PERFORMANCE WITH THE DEVICE WAS AFFECTED AFTER A TRAUMA TO THE HEAD. THE USER HAD NO HEARING SENSATION WITH THE DEVICE ANYMORE. THE USER WAS REIMPLANTED ON (B)(6) 2023.

    Patient problems: Failure of Implant

    MAUDE report 16756143 ↗

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-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. Mi1000 CONCE
  • 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 Product
  • 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

Other Implant, Cochlear devices

All Implant, Cochlear devices →

Sources and updates

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