| Subject: | FDA Announces Class I Recall of Alcon Refractive Horizons, Inc. LADAR6000 Excimer Laser System |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 6 Jun 2007 - 10:00 am |
| Alcon Refractive Horizons and the FDA have notified healthcare professionals and patients of a Class I Recall of the LADAR6000 Excimer Laser System for CustomCornea algorithm for myopia with astigmatism (M3) and myopia without astigmatism (A7). This system is used for LASIK and wave-front guided LASIK treatment for the reduction or elimination of mild to moderate nearsightedness (myopia) and farsightedness (hyperopia) with or without astigmatism or for mixed astigmatism in patients... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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