Model Number N/A |
Device Problem
Tear, Rip or Hole in Device Packaging (2385)
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Patient Problem
No Patient Involvement (2645)
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Event Date 12/05/2019 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).Udi # (b)(4).Foreign report source: (b)(6).Customer has indicated that the product is in process of being returned to zimmer biomet for investigation.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: 0001825034 - 2019 - 05715, 0001825034 - 2019 - 05717, 0001825034 - 2019 - 05718.
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Event Description
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It was reported during inspection of the circulated items in the warehouse, it was discovered inner sterile packages were damaged.No hospitals or patients were involved.Attempts have been made and additional information on the reported event is unavailable at this time.
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Event Description
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Upon reassessment of the reported event, it was determined to be not reportable.The initial report was forwarded in error and should be voided.
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Manufacturer Narrative
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Upon reassessment of the reported event, it was determined to be not reportable.The initial report was forwarded in error and should be voided.
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Search Alerts/Recalls
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