Every recall we track for Carl Zeiss Meditec AG — 7 in all — plus the complaints and injury reports the public filed about them.
Carl Zeiss Meditec recalls specific Zeiss Intrabeam Spherical Applicators due to failing to meet manufacturing specifications. Affected units include certain serial numbers and batch numbers. Consumers should contact the manufacturer for details.
ZEISS miLOOP Lens Fragmentation Device (model 303071-9090-000) used in cataract surgery may stick due to high friction. Affected units sold in 2011-2023; recall issued for safety.
Carl Zeiss Meditec recalls IOLMaster 700 devices with specific software versions due to potential patient data mismatch during patient list selection. Affected units may need software update or correction.
Carl Zeiss Meditec recalls VISULENS 550 devices with serial numbers pending due to potential electrical shock from a faulty communication board. Affected units may need repair or replacement.
Carl Zeiss Meditec recalls VISUREF150 eye diagnostic devices with serial numbers pending due to faulty DC/DC converter causing electrical shock risk. Affected units may have increased current leakage.
Carl Zeiss Meditec recalls IOLMaster 700 devices with serial number 1185393 due to incorrect calibration causing inaccurate eye imaging. Affected units may provide wrong measurements for eye surgery planning.
