--- title: "Arthrex, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Arthrex, 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/arthrex-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Arthrex, Inc. recall records **1** reported ongoing 2 records in this archive. Latest source date Nov 2, 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 Nov 2, 2022 FDA device enforcement ### [Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a cannulated reamer, sterile.](https://isitonrecall.com/recall/fda-device-z-0465-2023-small-joint-oats-set-ref-ar-8981-06s-6mm-and-small-joint-oats-set-ref-ar-8981-08s-8mm-both-containin/) The devices may be packaged with the wrong reamer size. Class II Reported ongoing Distribution: Distribution was made to AL, AR, CA, CO, FL, IA, IL, LA, MA, MD, MI, NC, NJ, NY, OH, PA, SC, TX, UT, and VA. There was no military/government distribution. Foreign distribution ... [Official source for Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0465-2023%22) Mar 25, 2022 FDA device enforcement ### [K-Wire, 1.35 mm x 170 mm](https://isitonrecall.com/recall/fda-device-z-1035-2022-k-wire-1-35-mm-x-170-mm/) Products do not meet length and diameter specifications. Class II Reported terminated Distribution: Worldwide distribution - US Nationwide distribution in the states of OH, TN, MO, LA, IA, AZ, PA, NY, OR and the countries of to Belgium, Egypt, Finland, France, Germany, Italy, ... [Official source for K-Wire, 1.35 mm x 170 mm](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1035-2022%22) ## Reasons in these listed records - The devices may be packaged with the wrong reamer size. - Products do not meet length and diameter specifications. These examples come from this result page and are not a ranking of every recall reason. ## Checking Arthrex, Inc. ### Is there a recall on arthrex, inc. right now? This archive contains 2 records, including 1 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 Arthrex, Inc.](https://isitonrecall.com/check/?q=Arthrex%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)