Model Number N/A |
Device Problems
Entrapment of Device (1212); Unstable (1667); Positioning Problem (3009)
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Patient Problems
Pain (1994); Swelling (2091); No Code Available (3191)
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Event Date 01/06/2015 |
Event Type
Injury
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Manufacturer Narrative
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Concomitant medical products - unknown head, unknown liner, fitmore hip stem a size 5/ pn 01.00551.105/ ln 2605633.Once the investigation has been completed, a follow up mdr will be submitted.Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2017-03357, 0001822565-2017-03359.
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Event Description
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It was reported that patient underwent total hip procedure and was revised due to pain, swelling, instability and problems sitting following a revision.All components were removed and replaced.
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Manufacturer Narrative
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This follow-up report is being submitted to relay additional information.Reported event was unable to be confirmed due to limited information received from the customer.Design history records was reviewed and no discrepancies were found.Review of the complaint history determined that no further action is required as no were trends identified.Root cause was unable to be determined as the necessary information to adequately investigate the reported event was not 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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Manufacturer Narrative
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This follow-up report is being submitted to relay additional information.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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Manufacturer Narrative
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This follow-up report is being submitted to relay additional information.Concomitant medical products: screw bone 6.5 mm dia x 25 mm catalog#: 62506525 lot#: 62444801.Continuum longevity elevated liner, gg 32 x 48 catalog#: 00875200832 lot#: 62521246.Biolox delta fem head, 32 mm, +3.5 mm catalog#: 00877503203 lot#: 2568102.Fitmore hip stem a, size 5 catalog#: 0100551105 lot#: 2605633.(b)(4).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 underwent total hip procedure and was revised due to pain, swelling, instability and problems sitting following a revision.Head, cup, screw and liner were removed and replaced.Revision operative record received indicated the revision was due to iliopsoas tendon impingement cause by anterior cup overhang.Attempts have been made and additional information on the reported event is unavailable.
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Manufacturer Narrative
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Reported event was confirmed by review of the revision op notes.Revision op notes provided the reason for the revision was due to iliopsoas tendon impingement from anterior cup over hang.Dhr was reviewed and no discrepancies were found.Review of the complaint history determined that no further action is required.Root cause was unable to be determined as the necessary information to adequately investigate the reported event was not 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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Search Alerts/Recalls
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