Catalog Number 47225500800 |
Device Problem
Unsealed Device Packaging (1444)
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Patient Problem
No Patient Involvement (2645)
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Event Type
malfunction
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Manufacturer Narrative
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(b)(4).Report source: foreign: (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 report will be submitted.Product not returned.
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Event Description
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It was reported that during an inspection at the warehouse, the packaging on the sterile products were found to be opened.There was no patient involvement.
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Manufacturer Narrative
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(b)(4).This follow-up report is being submitted to relay additional information.Void - after investigation/reassessment, the item was determined to be not reportable.
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Event Description
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No further event information available at the time of this report.
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Search Alerts/Recalls
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