Model Number N/A |
Device Problem
Packaging Problem (3007)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 11/07/2023 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).Customer has indicated that the product will not be returned to zimmer biomet for investigation, as its location is unknown.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.
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Event Description
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It was reported that during a knee procedure, the tibial insert was noted to have debris on it.No adverse events have been reported as a result of the malfunction.
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Manufacturer Narrative
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Upon reassessment of the reported event, it was determined an mdr should not have been filed under the current mfr number.This event will be reported on 3007963827-2024-00002.
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Event Description
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Upon reassessment of the reported event, it was determined an mdr should not have been filed under the current mfr number.This event will be reported on 3007963827- 2024-00002.
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Search Alerts/Recalls
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