Catalog Number 8065990713RP |
Device Problems
Improper or Incorrect Procedure or Method (2017); Improper Device Output (2953)
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Patient Problem
No Code Available (3191)
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Event Date 09/13/2015 |
Event Type
Injury
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Manufacturer Narrative
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Additional information has been requested.Investigation, including root cause analysis, is in progress.A supplemental mdr will be filed as necessary in accordance with 21 cfr 803.56 when additional reportable information becomes available.The manufacturer internal reference number is: (b)(4).
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Event Description
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A surgeon reported an energy fluctuation during lasik treatment.He reports post lasik treatment the patients left eye is undercorrected.Additional information has been requested.
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Manufacturer Narrative
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The manufacturer internal reference number is: (b)(4).
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Event Description
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Upon additional follow up it was reported that the patient underwent treatment for both eyes but it was the right eye that was under corrected.
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Manufacturer Narrative
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No abnormalities that could have contributed to this event were found during the device history records review and the product was released according to compay acceptance criteria.The reported event could not be confirmed.The manufacturer internal reference number is: (b)(4).
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Search Alerts/Recalls
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