Carl Zeiss Meditec AG
7 recalls on record · Latest: May 4, 2022
FDA Devices Moderate May 4, 2022
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
FDA Devices Moderate Feb 24, 2021
IOLMaster 700
FDA Devices Moderate Dec 23, 2020
Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objective refractive values and kerat…
FDA Devices Moderate Oct 24, 2018
Carl Zeiss Meditec AG, Goeschwitzer Strasse 51-52 07745 Jena, Germany, IOLMaster 700, REF 1932-169 SN 1185393 2017-09-01
FDA Devices Moderate Oct 11, 2017
Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABEAM System is…
FDA Devices Moderate Dec 9, 2015
IOL Master 500: Software versions 7.5 and 7.7; Ophthalmic: IOL Master 500 is intended for biometric determination of ocular measurements of axial …
FDA Devices Moderate Mar 19, 2014