--- title: "DePuy Mitek, Inc., a Johnson & Johnson Co. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search DePuy Mitek, Inc., a Johnson & Johnson Co. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/depuy-mitek-inc-a-johnson-johnson-co/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # DePuy Mitek, Inc., a Johnson & Johnson Co. recall records **7** reported ongoing 7 records in this archive. Latest source date Feb 24, 2025. 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 24, 2025 FDA device enforcement ### [COR Disposable Kit, 8 mm. Cartilage Transplant System.](https://isitonrecall.com/recall/fda-device-z-1314-2025-cor-disposable-kit-8-mm-cartilage-transplant-system/) Device is missing the pin in the graft loader component. Class II Reported ongoing Distribution: Domestic: Nationwide Distribution; Foreign: Austria, Belgium, Brazil, Switzerland, Chile, China, Colombia, Czech Republic, Germany, Spain, Finland, France, French Guyana, Greece... [Official source for COR Disposable Kit, 8 mm. Cartilage Transplant System.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1314-2025%22) Feb 24, 2025 FDA device enforcement ### [COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.](https://isitonrecall.com/recall/fda-device-z-1315-2025-cor-disposable-kit-8-mm-w-perpendicularity-cartilage-transplant-system/) Device is missing the pin in the graft loader component. Class II Reported ongoing Distribution: Domestic: Nationwide Distribution; Foreign: Austria, Belgium, Brazil, Switzerland, Chile, China, Colombia, Czech Republic, Germany, Spain, Finland, France, French Guyana, Greece... [Official source for COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1315-2025%22) Apr 13, 2023 FDA device enforcement ### [DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212724](https://isitonrecall.com/recall/fda-device-z-1677-2023-depuy-mitek-bioknotless-plus-w-ethibond-iindicated-for-use-in-soft-tissue-to-bone-fixation-in-associ/) IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS¿ Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS¿ Anchor inserter tip detected dur... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, Switzerland, China, Czech Republic, Germany, Egypt, Spain, United Kingdom, Hong Kong, Hun... [Official source for DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft tissue to bone fixation in as...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1677-2023%22) Apr 13, 2023 FDA device enforcement ### [DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212725](https://isitonrecall.com/recall/fda-device-z-1678-2023-depuy-mitek-bioknotless-plus-w-panacryl-indicated-for-use-in-soft-tissue-to-bone-fixation-in-associa/) IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS¿ Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS¿ Anchor inserter tip detected dur... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, Switzerland, China, Czech Republic, Germany, Egypt, Spain, United Kingdom, Hong Kong, Hun... [Official source for DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in ass...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1678-2023%22) Apr 13, 2023 FDA device enforcement ### [DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212726](https://isitonrecall.com/recall/fda-device-z-1679-2023-depuy-mitek-bioknotless-plus-w-oc-indicated-for-use-in-soft-tissue-to-bone-fixation-in-association-w/) IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS¿ Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS¿ Anchor inserter tip detected dur... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, Switzerland, China, Czech Republic, Germany, Egypt, Spain, United Kingdom, Hong Kong, Hun... [Official source for DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in associati...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1679-2023%22) Apr 13, 2023 FDA device enforcement ### [DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212722](https://isitonrecall.com/recall/fda-device-z-1680-2023-depuy-mitek-bioknotless-rapid-w-oc-indicated-for-use-in-soft-tissue-to-bone-fixation-in-association/) IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS¿ Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS¿ Anchor inserter tip detected dur... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, Switzerland, China, Czech Republic, Germany, Egypt, Spain, United Kingdom, Hong Kong, Hun... [Official source for DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in associat...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1680-2023%22) Apr 13, 2023 FDA device enforcement ### [DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization Model Number: 212723](https://isitonrecall.com/recall/fda-device-z-1681-2023-depuy-mitek-bioknotless-rapid-w-pan-indicated-for-use-in-soft-tissue-to-bone-fixation-in-association/) IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS¿ Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS¿ Anchor inserter tip detected dur... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, Switzerland, China, Czech Republic, Germany, Egypt, Spain, United Kingdom, Hong Kong, Hun... [Official source for DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft tissue to bone fixation in associa...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1681-2023%22) ## Reasons in these listed records - Device is missing the pin in the graft loader component. - IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS¿ Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS¿ Anchor inserter tip detected during surgery may requ... These examples come from this result page and are not a ranking of every recall reason. ## Checking DePuy Mitek, Inc., a Johnson & Johnson Co. ### Is there a recall on depuy mitek, inc., a johnson & johnson co. right now? This archive contains 7 records, including 7 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 DePuy Mitek, Inc., a Johnson & Johnson Co.](https://isitonrecall.com/check/?q=DePuy%20Mitek%2C%20Inc.%2C%20a%20Johnson%20%26%20Johnson%20Co.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)