--- title: "K2M, Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search K2M, 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/k2m-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # K2M, Inc recall records **3** reported ongoing 3 records in this archive. Latest source date Jun 13, 2022. 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 Jun 13, 2022 FDA device enforcement ### [Yukon Straight Rod 4.0 x120mm; Cat# 7601-540120. Used to provide immobilization and stabilization of spinal segments.](https://isitonrecall.com/recall/fda-device-z-1307-2022-yukon-straight-rod-4-0-x120mm-cat-7601-540120-used-to-provide-immobilization-and-stabilization-of-sp/) Some of the rods in this lot were observed to have discoloration, later confirmed to be indication of trace amounts of inorganic phosphorous compound. This may produce a mild irritating or inflammatory response; adverse local tissue reactions may occur rela... Class II Reported ongoing Distribution: Domestic distribution to FL GA NE NV NY OH OK SC Foreign distribution to Canada, EU, and Hong Kong. [Official source for Yukon Straight Rod 4.0 x120mm; Cat# 7601-540120. Used to provide immobilization and stabilization...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1307-2022%22) Jan 13, 2022 FDA device enforcement ### [Everest MI XT Inner Dilator, Catalog Number 5101-90167](https://isitonrecall.com/recall/fda-device-z-0705-2022-everest-mi-xt-inner-dilator-catalog-number-5101-90167/) Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting together properly during a surgical procedure. Some dilators from these lots and from other lots were subsequently determined to be affected by a manufa... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide. [Official source for Everest MI XT Inner Dilator, Catalog Number 5101-90167](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0705-2022%22) Jan 13, 2022 FDA device enforcement ### [Everest MI XT Outer Dilator, Catalog Number 5101-90168](https://isitonrecall.com/recall/fda-device-z-0706-2022-everest-mi-xt-outer-dilator-catalog-number-5101-90168/) Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting together properly during a surgical procedure. Some dilators from these lots and from other lots were subsequently determined to be affected by a manufa... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide. [Official source for Everest MI XT Outer Dilator, Catalog Number 5101-90168](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0706-2022%22) ## Reasons in these listed records - Some of the rods in this lot were observed to have discoloration, later confirmed to be indication of trace amounts of inorganic phosphorous compound. This may produce a mild irritating or inflammatory response; adverse local tissue reactions may occur related to cytotoxicity ... - Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting together properly during a surgical procedure. Some dilators from these lots and from other lots were subsequently determined to be affected by a manufacturing nonconformance. These examples come from this result page and are not a ranking of every recall reason. ## Checking K2M, Inc ### Is there a recall on k2m, inc right now? This archive contains 3 records, including 3 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 K2M, Inc](https://isitonrecall.com/check/?q=K2M%2C%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)