Model Number N/A |
Device Problem
Device Markings/Labelling Problem (2911)
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Patient Problem
No Information (3190)
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Event Date 01/11/2019 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).(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.
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Event Description
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During the procedure, it was reported that the package had a shorter screw than indicated on the label.The procedure was completed with product of another lot.No additional information available.
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Manufacturer Narrative
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Upon receipt of additional information, it has been determined that this device did not cause or contribute to the reported event.The initial report was forwarded in error and should be voided.
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Event Description
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Upon receipt of additional information, it has been determined that this device did not cause or contribute to a reportable event.The initial report was forwarded in error and should be voided.
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Search Alerts/Recalls
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