Catalog Number MB2XXX |
Device Problem
Physical Resistance/Sticking (4012)
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Patient Problem
Insufficient Information (4580)
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Event Type
malfunction
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Event Description
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It was reported on a social media post that a surgeon has seen a mobi-c implant stuck in kyphosis secondary to hypermobility.No further information has been received.
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Manufacturer Narrative
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Without a product return, no product evaluation is able to be conducted.The lot number is unknown; therefore the device history records are unable to be reviewed.Current information is insufficient to permit a valid conclusion about the cause of this event.If additional information is obtained that adds value to the relevant content of this report and/or a conclusion can be drawn, a follow-up report will be sent.
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Manufacturer Narrative
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Additional information in h6: component, investigation type, findings, and conclusions.Device evaluation: product was not returned and no photos were provided.A device evaluation was unable to be performed.Potential cause: root cause was unable to be determined.This event could possibly be attributed to operational or patient factors.Dhr review: dhr review unable to be performed as lot number is not known.Device use : this device is used for treatment.A follow-up report will be submitted if new information is received that changes the information provided in this report.
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Event Description
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It was reported on a social media post that a surgeon has seen a mobi-c implant stuck in kyphosis secondary to hypermobility.No further information has been received.
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Search Alerts/Recalls
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