Catalog Number 004551003 |
Device Problems
Device Inoperable (1663); Device Damaged Prior to Use (2284)
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Patient Problems
No Consequences Or Impact To Patient (2199); No Patient Involvement (2645)
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Event Date 03/21/2016 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The device sample was not returned for evaluation at the time of this report.
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Event Description
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The customer alleges that the device (blade) looked damaged, however once the blade was placed on the dispoled handle it did not work.The device was not used on a patient.
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Manufacturer Narrative
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(b)(4).The sample was not returned for evaluation; therefore, the complaint could not be confirmed.If the sample is returned, a follow-up report will be submitted with investigation results.
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Event Description
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The customer alleges that the device (blade) looked damaged, however once the blade was placed on the dispoled handle it did not work.The device was not used on a patient.
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Search Alerts/Recalls
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