Overview of recall records associated with MED-EL Elektromedizinische Gereate, Gmbh, including dates, categories and classifications where available.
Classification mix: Class II: 4.
A small number of devices may have a higher probability of a crack within the internal electronics substrate which could result in a non-functional device.
Devices were distributed despite the Helium-fine leak test results not being within the cochlear implant standards specification.
Devices were distributed despite the Helium-fine leak test results not being within the cochlear implant standards specification.
Devices were distributed despite the Helium-fine leak test results not being within the cochlear implant standards specification.
This page summarizes recall records in which the official source identifies MED-EL Elektromedizinische Gereate, Gmbh as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
