RecallRadar

FDA Device recall Z-2138-2019

MED EL Cochlear Implant System, PULSARci100 Standard - Product Usage: The PULSARci100 Implant is an implantable part of the MED EL Cochlear…

On 2019-08-14 the FDA classified a Class II recall of MED EL Cochlear Implant System, PULSARci100 Standard - Product Usage: The PULSARci100 Implant is an implantable part of the MED EL Cochlear… by Med El Elektromedizinische Gereate, citing devices were distributed despite the Helium-fine leak test results not being within the cochlear implant standards specification.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2138-2019
ClassificationClass II
Statusterminated
Initiated2018-10-16
Published2019-08-14
Last updated2026-09-13 11:55 UTC
CompanyMed El Elektromedizinische Gereate
DistributionUS

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.

Reason

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

Identifiers

code_infoSerial Number 202001

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2138-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.