Catalog Number 115396 |
Device Problem
Fracture (1260)
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Patient Problem
Erosion (1750)
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Event Date 08/23/2022 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).Multiple mdr reports were filed for this event, please see associated reports: 0001825034-2022-02126; 0001825034-2022-02128.Device product code - phx.Concomitant medical products: item# 115330; lot# 185040; item# 180552; lot# 763020; item# 180552; lot# 905490; item# 110030777; lot#11024237; item#110031400; lot# 65095786; item# 110031421; lot# 64343831; item#118001; lot# j7192948; item#113077; lot# 314170.Customer has indicated that the product will not be returned to zimmer biomet for investigation, as the product was requested but not returned by the hospital.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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Event Description
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It was reported that patient was revised approximately one (1) year and two (2) months post-implantation due to no fixation of the baseplate and two (2) fractured screws.During the procedure, the baseplate, glenosphere, poly and screws were removed and patient was converted to a hemi shoulder.Attempts have been made and no further information has been provided.
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Event Description
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No further event information available at the time of this report.
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Manufacturer Narrative
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This follow-up report is being submitted to relay additional information.Visual examination of the provided photographs identified the implants that were explanted.A central screw and peripheral screw appear broken.Radiographs were provided and reviewed by a health care professional.Review of the available records identified the following: significant findings include a fractured central screw of the glenoid component is identified.No contribute factors are seen.Review of the device history record(s) identified no deviations or anomalies during manufacturing.A definitive root cause cannot be determined.If any further information which would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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Search Alerts/Recalls
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