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CALLISTO eye

Carl Zeiss Meditec AG · Model CALLISTO eye · UDI-DI 04049539104366

NFJ Prescription
10
510(k) clearances
47
Adverse events
14
Recalls
31
Facilities

Recalls

DateFirmReason
2025-09-09MedicalCommunications GmbHPotential that the measured value may be smaller than the actual area.
2024-09-17Topcon Medical Systems, Inc.The overlay of visual field test locations on a probability map, as presented in IMAGEnet 6 in the so-called "Hood Report", is not appropriate as it can imply a structure/function
2022-01-11Diagnos IncRetinal analysis system software has some features, based on artificial intelligence, that potentially lack appropriate market approval, so it is recommended to use a specific prio
2020-12-18Topcon Medical Systems, Inc.Harmony RS integrations with Topcon equipment, TRC NW-400 and the Signal Camera, allowed user input of non-unique patient IDs that caused multiple patient records and images to be
2020-11-03Kowa Optimed IncIt has been determined that the software distributed with the retinal camera may delete patient information. Specifically, if multiple IDs are delated at the same time, their is a
2019-03-06Topcon Medical Systems, Inc.When a patient is selected in the patient data and another patient is selected prior to the display of the primary patient's thumbnails is completed, then the primary patient's thu
2017-06-13Merge Healthcare, Inc.When the user has not set up any user preference on the sorting order to render the study images (OS/OD/etc.) and reports, the ECP may get an incorrect study index. If the user att
2017-01-05Haag-Streit USA IncThere is a possibility for data to be stored under the wrong patient on the DICOM Server following a non-standard workflow.
2016-04-04Merge Healthcare, Inc.The system will completely stop allowing the downloading or acquisition of new images due to incompatible software application versions.
2016-04-04Merge Healthcare, Inc.During an antivirus program scan of the Eye Station or Eye Care PACS, the antivirus program may detect a newly captured image to be an unwanted file and delete the image permanentl

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.