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All product recalls associated with VISX INCORPORATED, A SUBSIDIARY OF AMO INC.
Total Recalls
4
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.
Erroneous Treatment Calculations - Two software caused errors; in combination, in the WaveScan System Software, will result in an erroneous treatment calculation (overcorrection) in patients. (1) Installation of software for a certain brand of computer (Dedicated Computing LLC) can cause a software registry setting for an algorithm that identifies image reflection to be erroneously set in the "off