Carl Zeiss Meditec AG recalls

9 recalls on record · latest: March 16, 2022

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

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Carl Zeiss Meditec AG recalls ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.

March 16, 2022 · Medical device recalls Moderate risk High friction of the slider can cause the device to stick, or not move as inten…

Carl Zeiss Meditec AG recalls IOLMaster 700

December 7, 2020 · Medical device recalls Moderate risk When using software 1.90.2.09 or 1.90.8.06 and using modality worklist function…

Carl Zeiss Meditec AG recalls Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objecti…

August 6, 2020 · Medical device recalls Moderate risk Due to the incorrect DC/DC converter being assembled onto the communication boa…

Carl Zeiss Meditec AG recalls Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of cont…

August 6, 2020 · Medical device recalls Moderate risk Due to the incorrect DC/DC converter being assembled onto the communication boa…

Carl Zeiss Meditec AG recalls Carl Zeiss Meditec AG, Goeschwitzer Strasse 51-52 07745 Jena, Germany, IOLMaster 700, REF 1932-169 SN 1185393 2017-09-01

June 25, 2018 · Medical device recalls Moderate risk Calibration setting was incorrectly entered during manufacturing causing the op…

Carl Zeiss Meditec AG recalls Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germ…

August 30, 2017 · Medical device recalls Moderate risk The device had an incorrect printed calibration value on the calibration certif…

Carl Zeiss Meditec AG recalls IOL Master 500: Software versions 7.5 and 7.7; Ophthalmic: IOL Master 500 is intended for biometric determination of oc…

October 27, 2015 · Medical device recalls Moderate risk IOL Master software versions 7.5 and 7.7 calculation printouts and exported rep…

Carl Zeiss Meditec AG recalls IOL Master 5.5: Software versions 7.5 and 7.7; Ophthalmic: used to obtain ocular measurements and perform calculations…

October 27, 2015 · Medical device recalls Moderate risk IOL Master software versions 7.5 and 7.7 calculation printouts and exported rep…

Carl Zeiss Meditec AG recalls FORUM Archive and Viewer, version 3.1, v 3.1.1, (DVD Format) and v 3.2, v 3.2.1.(DVD and USB Flash Drive Format). Catal…

January 22, 2015 · Medical device recalls Moderate risk Software defect in the FORUM Viewer versions 3.1 and 3.2 which may lead to misi…