Model Number N/A |
Device Problems
Adverse Event Without Identified Device or Use Problem (2993); Noise, Audible (3273)
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Patient Problems
Fall (1848); Pain (1994); Ambulation Difficulties (2544); Joint Laxity (4526)
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Event Date 10/12/2021 |
Event Type
Injury
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Event Description
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It was reported that the patient underwent a left unicompartmental knee arthroplasty revision to address medial collateral ligament sprain, continued pain and ligament instability following a fall approximately nine (9) months post-operatively.Initial operative notes noted no intraoperative complications.Revision operative notes noted the patient had worsening pain, increasing functional limitations and there was a concern for ligamentous instability.No intraoperative complications were noted.Attempts have been made; however, no additional information is available.
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Manufacturer Narrative
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(b)(4).D10 concomitant devices unknown persona partial knee femur size 1 catalog #: ni, lot #: ni.Unknown personal partial knee vivacit-e polyethylene articular surface 10mm catalog #: ni, lot #: ni.Unknown personal partial knee tibial tray size c catalog #: ni, lot #: ni.Unknown bone cement catalog #: ni, lot #: ni.The complainant has indicated that the product will not be returned to zimmer biomet for investigation, as the device was discarded.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.Multiple mdr reports were filed for this patient; please see all reports associated with this event: 0001825034-2023-02239.H3 other text : investigation incomplete.
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Manufacturer Narrative
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This follow-up report is being filed to relay additional information.D10 - concomitant devices - persona partial knee cemented femoral component size 1 left medial catalog #: 42558000101.Lot #: 64386211, persona partial knee cemented tibial component size c left medial catalog #: 42538000301.Lot #: 64468722, biomet bone cement r 1x40.Catalog #: 110035368.Lot #: 004aac2502.
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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.Medical records provided were reviewed and the reported event was confirmed.The device history records were reviewed and no discrepancies were identified.A definitive root cause could not be determined with the information provided.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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No further event information available at the time of this report.
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Search Alerts/Recalls
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