--- title: "Orthalign, Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Orthalign, Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/orthalign-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Orthalign, Inc recall records **2** reported ongoing 2 records in this archive. Latest source date Feb 10, 2026. 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 Feb 10, 2026 FDA device enforcement ### [Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System](https://isitonrecall.com/recall/fda-device-z-1629-2026-drill-plate-ortho-dev-trimax-pegged-pref-size-1-5-ref-402566-component-lantern-knee-system/) Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) Class II Reported ongoing Distribution: US Nationwide distribution in the state of UT. [Official source for Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1629-2026%22) Feb 10, 2026 FDA device enforcement ### [Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System](https://isitonrecall.com/recall/fda-device-z-1630-2026-drill-plate-ortho-dev-trimax-pegged-pref-size-6-7-ref-402567-component-lantern-knee-system/) Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) Class II Reported ongoing Distribution: US Nationwide distribution in the state of UT. [Official source for Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1630-2026%22) ## Reasons in these listed records - Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) These examples come from this result page and are not a ranking of every recall reason. ## Checking Orthalign, Inc ### Is there a recall on orthalign, inc right now? This archive contains 2 records, including 2 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 Orthalign, Inc](https://isitonrecall.com/check/?q=Orthalign%2C%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)