medical Class II Updated 2019-08-14

MED-EL Elektromedizinische Gereate, Gmbh recalls MED EL Cochlear Implant System, PULSARci100 Standard - Produ

Recalled Product

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 together with compatible MED EL external components. The MED EL Cochlear Implant System is intended to evoke auditory sensations via electrical stimulation of the auditory pathways for severely to profoundly hearing impaired individuals who obtain little or no benefit from acoustic amplification in the best aided condition.


Hazard / Issue

Devices were distributed despite the Helium-fine leak test results not being within the cochlear implant standards specification.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Serial Number 202001
View official government recall

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