FDA recall record

MED-EL Elektromedizinische Gereate, Gmbh MED EL Cochlear Implant System, PULSARci100 recall — FDA Z-2138-2019

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

Class IIclassification
Z-2138-2019official record ID
Aug 14, 2019report date

Recall record at a glance

Official recordZ-2138-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMED-EL Elektromedizinische Gereate, Gmbh
Report dateAug 14, 2019
Recall initiation dateOct 16, 2018
Quantity1 device
LocationInnsbruck, N/A, Austria

Official product description

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.

Why the product was recalled

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

Distribution information

Worldwide distribution - US Nationwide in the states of California and Illinois. Countries of ARGENTINA, AUSTRALIA, AUSTRIA, BRAZIL, BULGARIA, CHINA, FRANCE, GEORGIA, KOREA, REPUBLIC OF, POLAND, RUSSIAN FEDERATION, SPAIN, SWEDEN.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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