Carl Zeiss Meditec, Inc.: Medical Device Recalls in 2020

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Carl Zeiss Meditec, Inc. in 2020. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

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The PLEX Elite 9000, a Swept-Source OCT [SS-OCT] - Product Usage: The PLEX Elite 9000 Swept-Source OCT [SS-OCT] is a non- contact, high resolution, wide field of view tomographic and biomicroscopic imaging device intended for in-vivo viewing, axial cross-sectional and three-dimensional imaging of posterior ocular structures. The device is indicated for visualizing posterior ocular structures including, but not limited to, retina, retinal nerve fiber layer, ganglion cell plus inner plexiform layer, macula, optic nerve head, vitreous and choroid. The PLEX Elite SS-OCT angiography is indicated as an aid in the visualization of vascular structures of the retina and choroid.