FDA Announces Class I Recall of Ophthalmic Surgical Device

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Title: FDA Announces Class I Recall of Ophthalmic Surgical Device

FDA Announces Class I Recall of Ophthalmic Surgical Device
Fri, 02 Jan 2009 08:22:00 -0600

The U.S. Food and Drug Administration announced a Class I recall of lot no. UD30654 of Healon D, an ophthalmic viscosurgical device (OVD) manufactured by Advanced Medical Optics Inc. (AMO) of Santa Ana, Calif.


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