http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.cfm

At the product code type in LZS for lasers, or HNO for microkeratomes. For Intralase (Intra-LASIK) type "Intra" for the Manufacturer.

It's pitiful that so few people know to file MDRs to report adverse events. If only 1% of patients experienced an adverse event and filed an MDR, there should be tens of thousands of adverse events reported. That would have gotten the FDA's attention.

Filing an MDR is sort of like voting. If you don't vote, you can't complain about who gets elected. If you don't file your MDR, you can't complain that the FDA is not doing anything about all of the problems.

Please file your MDR.

http://www.fda.gov/medwatch/report/consumer/consumer.htm

PTT