Carl Zeiss Meditec, Inc. recalls

4 recalls on record · latest: January 14, 2022

Official U.S. recall history for Carl Zeiss Meditec, Inc., compiled from official government records.

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Carl Zeiss Meditec, Inc. recalls CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex

January 14, 2022 · Medical device recalls Moderate risk Optic nerve head angiography scan to be turned off due to its distribution with…

Carl Zeiss Meditec, Inc. recalls Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"

July 8, 2021 · Medical device recalls Moderate risk Due to failure to acquire pre-market clearance for its high resolution tomograp…

Carl Zeiss Meditec, Inc. recalls VisuMax Software Version 2.10.13 with activated Software-Module ReLEx (SMILE) option used in conjunction with the VisuM…

December 6, 2018 · Medical device recalls Moderate risk VisuMax devices with software version 2.10.13 and activated SW-Module ReLEx (SM…

Carl Zeiss Meditec, Inc. recalls The PLEX Elite 9000, a Swept-Source OCT [SS-OCT] - Product Usage: The PLEX Elite 9000 Swept-Source OCT [SS-OCT] is a no…

October 16, 2018 · Medical device recalls Moderate risk Under certain fault conditions, the existing design may expose the operator to…