Catalog Number 244000561 |
Device Problem
Crack (1135)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 07/05/2018 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Event Description
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Medial device reprocessing department identified that item 244000561 had become cracked, and was no longer functional.The item was discarded.A replacement is required.No further information is available.Please send replacement item direct to the customer at: (b)(6).No charge shipping (b)(4).Please confirm eta of replacement.Thank you.Patient consequence? no.Is the information being submitted for this complaint all the details that are known/available regarding this event? yes.
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Manufacturer Narrative
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(b)(4).Investigation summary: the instrument associated with this report was not returned.Depuy considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.If information is obtained that was not available for the initial medwatch , a follow-up medwatch will be filed as appropriate.
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Search Alerts/Recalls
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