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AMO Puerto Rico Manufacturing Recalls
19 recalls on record · March 12, 2014 to April 1, 2026 · Medical Devices
Recalls by year
14
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 1, 2026Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name: TECNIS Eyhance IOL with TECNIS Sim
Hazard: Due to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as consistently as expected.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
August 27, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual
Hazard: Units may be labeled with the incorrect diopter power.
March 12, 2014Medical DevicesFDA
AMO Puerto Rico Manufacturing, Inc. recalls AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002, diopter size: 16.0 and 21.0. Indicated for pri
Hazard: Certain Silicone TECNIS IOLs may be labeled with the incorrect diopter power.