--- title: "Oculus Optikgeraete GMBH Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Oculus Optikgeraete GMBH recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/oculus-optikgeraete-gmbh/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Oculus Optikgeraete GMBH recall records **6** reported ongoing 6 records in this archive. Latest source date Aug 8, 2023. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. 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/). ## Records and reported status Aug 8, 2023 FDA device enforcement ### [Oculus Pentacam AXL Wave, Ref 70020, CE 0123](https://isitonrecall.com/recall/fda-device-z-2482-2023-oculus-pentacam-axl-wave-ref-70020-ce-0123/) Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, FL, MA, MN, NY, NC, OH, PA, TX, VA, WA. OUS: Not Provided [Official source for Oculus Pentacam AXL Wave, Ref 70020, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2482-2023%22) Aug 8, 2023 FDA device enforcement ### [Oculus Pentacam AXL , Ref 70100, CE 0123](https://isitonrecall.com/recall/fda-device-z-2483-2023-oculus-pentacam-axl-ref-70100-ce-0123/) Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, FL, MA, MN, NY, NC, OH, PA, TX, VA, WA. OUS: Not Provided [Official source for Oculus Pentacam AXL , Ref 70100, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2483-2023%22) Aug 8, 2023 FDA device enforcement ### [Oculus Myopia Master , Ref 68100, CE 0123](https://isitonrecall.com/recall/fda-device-z-2484-2023-oculus-myopia-master-ref-68100-ce-0123/) Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, FL, MA, MN, NY, NC, OH, PA, TX, VA, WA. OUS: Not Provided [Official source for Oculus Myopia Master , Ref 68100, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2484-2023%22) Jul 8, 2022 FDA device enforcement ### [Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.](https://isitonrecall.com/recall/fda-device-z-1672-2022-pentacam-axl-wave-ref-70020-used-to-image-the-anterior-segment-of-the-eye/) Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs Class II Reported ongoing 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.... [Official source for Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1672-2022%22) Jul 8, 2022 FDA device enforcement ### [Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.](https://isitonrecall.com/recall/fda-device-z-1673-2022-pentacam-axl-ref-70100-pentacam-hr-ref-70900-used-to-image-the-anterior-segment-of-the-eye/) Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs Class II Reported ongoing 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.... [Official source for Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1673-2022%22) Jul 8, 2022 FDA device enforcement ### [Pentacam HR REF 70900. Used to image the anterior segment of the eye.](https://isitonrecall.com/recall/fda-device-z-1674-2022-pentacam-hr-ref-70900-used-to-image-the-anterior-segment-of-the-eye/) Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs Class II Reported ongoing 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.... [Official source for Pentacam HR REF 70900. Used to image the anterior segment of the eye.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1674-2022%22) ## Reasons in these listed records - Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements. - Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs These examples come from this result page and are not a ranking of every recall reason. ## Checking Oculus Optikgeraete GMBH ### Is there a recall on oculus optikgeraete gmbh right now? This archive contains 6 records, including 6 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Oculus Optikgeraete GMBH](https://isitonrecall.com/check/?q=Oculus%20Optikgeraete%20GMBH) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)