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Model Number N/A |
Device Problem
Migration or Expulsion of Device (1395)
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Patient Problem
No Information (3190)
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Event Date 10/28/2020 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).The device will not be returned for analysis as it was discarded; however, an investigation of the reported event is in progress.Once the investigation is completed, a supplemental medwatch 3500a will be submitted.The user facility is foreign; therefore, a facility medwatch report will not be available.Report source ¿ (b)(6).
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Event Description
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It was reported the patient underwent a sternum dissection after the sternal closure plate came off post-operatively.The surgeon speculated that the sternum was not cut correctly in the middle during the original surgery.Following the revision, the patient recovered and was transferred to another hospital.No additional patient consequences have been reported.
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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.No product was returned or pictures provided; visual and dimensional evaluations could not be performed.Lot identification is necessary for review of device history records, lot identification was not provided for the plate.A definitive root cause cannot be determined.It was reported: the doctor in charge speculated that it was probably because the sternum was not cut correctly in the middle.However, without medical records a definitive root cause cannot be determined.If any further information is found which would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.This report is being submitted to update additional information in section d10, h2, h3, h6 and h10.
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Search Alerts/Recalls
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