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Abbott Medical Optics, Inc. Recall: OptiMedica Catalys Precision Laser System; Model No(s)

Abbott Medical Optics, Inc. Recall: OptiMedica Catalys Precision Laser System; Model No(s) is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Abbott Medical Optics, Inc.; Product: OptiMedica Catalys Precision Laser System; Model No(s). Catalys-U (US), and Catalys-I (Outside US). Product U

Recalling firmAbbott Medical Optics, Inc.
ProductOptiMedica Catalys Precision Laser System; Model No(s). Catalys-U (US), and Catalys-I (Outside US). Product Usage: Indicated for use in patients undergoing cataract surgery for removal of crystalline lens.
Reason for recallDevice may experience loss of suction during treatment resulting in scoring the cornea during lens fragmentation.
ClassificationClass II (moderate — may cause temporary or reversible health consequences)
StatusTerminated
DistributionWorldwide Distribution - US Nationwide and the countries of, Canada, Germany, Switzerland, Australia, Spain, Japan, Great Britain, France, Netherlands, Austria, Singapore, South Korea, India, Thailand, Colombia, Ecuador, Italy, Brazil, Egypt, Tunsia, Belgium, Mexico, Greece, Guatemala, Chile, Turkey
Recall initiated20150220
Recall numberZ-1515-2015
Categorydevice
StateCA
CountryUnited States

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