Catalog Number 00631005032 |
Device Problems
Device Dislodged or Dislocated (2923); Unintended Movement (3026)
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Patient Problem
Joint Dislocation (2374)
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Event Date 01/29/2019 |
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: 0001822565-2023-00443.Concomitant medical products: cat#: 00801803201/lot#: 63593580 / femoral head sterile product do not resterilize 12/14 taper.Report source: brazil.The device will not be returned for analysis; however, an investigation of the reported event is in progress.Once the investigation is completed, a supplemental medwatch will be submitted.
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Event Description
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It was reported a patient underwent a closed reduction procedure to correct a dislocation.Attempts have been made and no further information is available.
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Manufacturer Narrative
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Upon receipt of additional information, it was determined this product should not have been reported under this mfr number.This report should be voided and a corrected report will be filed under mfr number: (b)(4).
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Event Description
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Upon receipt of additional information, it was determined this product should not have been reported under this mfr number.This report should be voided and a corrected report will be filed under mfr number: (b)(4).
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Search Alerts/Recalls
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