Model Number N/A |
Device Problem
Shipping Damage or Problem (1570)
|
Patient Problem
No Patient Involvement (2645)
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Event Type
malfunction
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Manufacturer Narrative
|
(b)(4).Product has been received by zimmer biomet and the investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.
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Event Description
|
It was reported by the distributor the product arrived damaged with sterility barrier potentially compromised.There was no patient involvement.
|
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Manufacturer Narrative
|
It was determined this device did not cause or contribute to a reportable malfunction, serious injury, or adverse event.Please void this submission.
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Event Description
|
It was determined this device did not cause or contribute to a reportable malfunction, serious injury, or adverse event.Please void this submission.
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Search Alerts/Recalls
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