--- title: "Pentacam HR REF 70900. Used to image the anterior segment of the eye. — FDA record Z-1674-2022 | Is It on Recall" description: "Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs" url: https://isitonrecall.com/recall/fda-device-z-1674-2022-pentacam-hr-ref-70900-used-to-image-the-anterior-segment-of-the-eye/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Pentacam HR REF 70900. Used to image the anterior segment of the eye. — FDA record Z-1674-2022 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Jul 8, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: Pentacam HR REF 70900. Used to image the anterior segment of the eye. - **Reason**: Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs - **Classification**: Class II - **Recalling firm**: Oculus Optikgeraete GMBH - **Quantity**: 19 systems with affected software - **Agency-reported status**: Ongoing - **Source record identifier**: Z-1674-2022 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1674-2022%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | Software version: 1.26r26 and 1.26r27 Model Number: 70900 UDI-DI Code: 04049584000026 Serial Numbers: 70900 0574 8160 70900 0925 0240 70900 0995 2250 70900 1664 8130 70900 1995 2250 70900 3451 7060 70900 3795 2250 70900 3965 1270 70900 4041 7010 70900 4172 2110 70900 4795 2250 70900 6234 7150 70900 7552 1160 70900 7952 1180 70900 8804 6140 70900 8813 3140 70900 9142 0121 70900 9695 2250 70900 9795 2250 | Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution U.S.: AL, AR, AZ, CAQ, CO, CT, FL, GA, HI, IA, ID, IL, KS, KY, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, PA, Puerto Rico, SC, SD, TN, TX, UT, VA, WA, WI, and WY O.U.S.: N/A States below are derived from the distribution text, including nationwide wording. 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These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1674-2022%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Oculus Optikgeraete GMBH records](https://isitonrecall.com/brand/oculus-optikgeraete-gmbh/)