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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: WAVELIGHT LASER TECHNOLOGIE AG ALLEGRETTO LASER LASIK LASER

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WAVELIGHT LASER TECHNOLOGIE AG ALLEGRETTO LASER LASIK LASER Back to Search Results
Event Date 09/22/2011
Event Type  No Answer Provided  
Event Description

Had lasik surgery with the allegretto system and now i have severe dry eye disease. No treatment is working and it is costing my family tons of money that i am on the verge of not wanting to live anymore, help.

 
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Brand NameALLEGRETTO LASER
Type of DeviceLASIK LASER
Manufacturer (Section D)
WAVELIGHT LASER TECHNOLOGIE AG
MDR Report Key3209163
Report NumberMW5030756
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 06/28/2013
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/28/2013
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel

Patient TREATMENT DATA
Date Received: 06/28/2013 Patient Sequence Number: 1
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