--- title: "Omnia Medical Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Omnia Medical recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/omnia-medical/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Omnia Medical recall records **2** reported ongoing 2 records in this archive. Latest source date Jul 15, 2024. 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 15, 2024 FDA device enforcement ### [TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 degree and 60 degree.](https://isitonrecall.com/recall/fda-device-z-2556-2025-tibrid-stand-alone-intervertebral-body-fusion-device-sa-angled-punch-awl-sizes-30-degree-45-degree-a/) Failure of fusion system instruments in the field. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NJ, NV, OK & WA. [Official source for TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 d...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2556-2025%22) Jul 15, 2024 FDA device enforcement ### [TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled Screwdrivers, Sizes 30 degree, 45 degree, and 60 degree angles.](https://isitonrecall.com/recall/fda-device-z-2557-2025-tibrid-stand-alone-intervertebral-body-fusion-device-tibrid-sa-angled-screwdrivers-sizes-30-degree-4/) Failure of fusion system instruments in the field. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NJ, NV, OK & WA. [Official source for TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled Screwdrivers, Sizes 30 deg...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2557-2025%22) ## Reasons in these listed records - Failure of fusion system instruments in the field. These examples come from this result page and are not a ranking of every recall reason. ## Checking Omnia Medical ### Is there a recall on omnia medical 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 Omnia Medical](https://isitonrecall.com/check/?q=Omnia%20Medical) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)