--- title: "restor3d Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search restor3d 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/restor3d-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # restor3d Inc. recall records **2** reported ongoing 5 records in this archive. Latest source date Jul 27, 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 Jul 27, 2026 FDA device enforcement ### [Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide), REF: 5831-9006](https://isitonrecall.com/recall/fda-device-z-3178-2026-kinos-axiom-total-ankle-system-with-axiom-psr-flat-cut-cut-guide-ref-5831-9006/) Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fixation or poor alignment of implants, implant loosening/migration, or need for... Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, CO. [Official source for Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide), REF: 5831-9006](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3178-2026%22) Jun 30, 2026 FDA device enforcement ### [Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog Number: 1500-1030; 1500-1035 Software Version: N/A - off-the-s...](https://isitonrecall.com/recall/fda-device-z-2987-2026-brand-name-veritas-standard-reverse-total-shoulder-product-name-veritas-standard-glenoid-baseplate-m/) Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the state of Texas. [Official source for Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Basepl...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2987-2026%22) Mar 30, 2022 FDA device enforcement ### [Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument](https://isitonrecall.com/recall/fda-device-z-1026-2022-non-sterile-double-ended-trial-kit-small-footprint-6110-n01-kts01-for-the-cervical-cage-the-kit-incl/) Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium. Class II Reported terminated Distribution: US Nationwide distribution in the states of KY, NC, NJ, TX, IN, VA and AL. [Official source for Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1026-2022%22) Mar 30, 2022 FDA device enforcement ### [Evans Wedge Disposable Trials, Medium Footprint, 10mm Thickness (6101-20181018). Orthopedic manual surgical instrument](https://isitonrecall.com/recall/fda-device-z-1027-2022-evans-wedge-disposable-trials-medium-footprint-10mm-thickness-6101-20181018-orthopedic-manual-surgic/) During re-work of disposable instruments to relabel for 4-year shelf-life of disposable instruments, parts got mixed into other lots. Class II Reported terminated Distribution: US Nationwide distribution in the states of KY, NC, NJ, TX, IN, VA and AL. [Official source for Evans Wedge Disposable Trials, Medium Footprint, 10mm Thickness (6101-20181018). Orthopedic manua...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1027-2022%22) Mar 30, 2022 FDA device enforcement ### [Evans Wedge Disposable Trials, Large Footprint, 8mm Thickness (Model: 6101-22200818). Orthopedic manual surgical instrument](https://isitonrecall.com/recall/fda-device-z-1028-2022-evans-wedge-disposable-trials-large-footprint-8mm-thickness-model-6101-22200818-orthopedic-manual-su/) During re-work of disposable instruments to relabel for 4-year shelf-life of disposable instruments, parts got mixed into other lots. Class II Reported terminated Distribution: US Nationwide distribution in the states of KY, NC, NJ, TX, IN, VA and AL. [Official source for Evans Wedge Disposable Trials, Large Footprint, 8mm Thickness (Model: 6101-22200818). Orthopedic ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1028-2022%22) ## Reasons in these listed records - Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fixation or poor alignment of implants, implant loosening/migration, or need for revision surgery. - Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws. - Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium. - During re-work of disposable instruments to relabel for 4-year shelf-life of disposable instruments, parts got mixed into other lots. These examples come from this result page and are not a ranking of every recall reason. ## Checking restor3d Inc. ### Is there a recall on restor3d inc. right now? This archive contains 5 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 restor3d Inc.](https://isitonrecall.com/check/?q=restor3d%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)