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All product recalls associated with VISX INCORPORATED, A SUBSIDIARY OF AMO INC.
Total Recalls
3
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2008
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Inaccurate measurements may be generated by the device, which could result in improper treatment and deterioration of patient eyesight.
Firm received two complaints (including one injury complaint) associated with the movement of the VISX chair while in the patient loading ("fully swung out" unlocked) position under an IntraLase FS laser.
Firm became aware of a significant overcorrection in one eye of a patient who had received a wavefront-guided LASIK treatment at a facility in Germany. The probability of a recurrence of this error was determined to be extremely remote. To ensure that this type of incident will not happen again, a software update was developed.