{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-08-15", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "196170", "product_res_number": "Z-0106-2023", "event_date_initiated": "2022-09-07", "event_date_posted": "2022-10-20", "recall_status": "Terminated", "event_date_terminated": "2026-03-04", "res_event_number": "90901", "product_code": "LRO", "product_description": "CENTURION SnagFree Chest Tube insertion Tray, Reorder CHT545", "code_info": "UDI/DI 20653160222979, Lot Code 2022050690", "firm_fei_number": "1417592", "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield", "address_1": "3 Lakes Dr", "city": "Northfield", "state": "IL", "postal_code": "60093-2753", "additional_info_contact": "Karin Johnson\n866-359-1704", "reason_for_recall": "One lot of chest tube insertion trays, containing a silk suture component that is restricted to 1 cycle of sterilization, was processed though 2 cycles.", "root_cause_description": "Under Investigation by firm", "action": "Medline Industries issued a Medical Device Recall note on 09/08/2022 by mail and email. The notice explained the problem and the potential hazard and requested the following: \n\"REQUIRED ACTION:\n1.Immediately check your stock for the affected item number and the affected lot numbers listed on the recall portal. Destroy affected product.\n2.Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the form.\nThe login for completing the response form is: Website link: https://recalls.medline.com Recall Reference #: R-22-131-FG Recall Code: RXXXXXXX\n3.Upon completion of the form, please destroy affected product. Your account will receive credit once the response form is submitted.\n4.If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. \n Have the customers document and destroy any affected product. You should include your customers quantities on your response form.\nIf you have any questions, please contact the Recall Department at 866-359-1704.\"", "product_quantity": "18 kits", "distribution_pattern": "US Nationwide distribution in the states of CA and TX.", "openfda": { "k_number": [ "K212258", "K934028", "K951149", "K894685", "K871873", "K963721", "K883250", "K890098", "K932217", "K881083", "K945160", "K962826", "K933137", "K920292", "K965201", "K884093", "K873973", "K923600", "K936117", "K910368", "K854292", "K934428", "K971062", "K871459", "K953083", "K041080", "K931759", "K874760", "K971061", "K890729", "K880961", "K930700", "K905459", "K023276", "K902293", "K935686", "K964921", "K931673", "K913136", "K935483", "K951478", "K914036", "K941846", "K874439", "K893814", "K914037", "K890570", "K213481", "K914174", "K914935", "K950574", "K871437", "K902887", "K880942", "K932652", "K970187", "K882684", "K945481", "K970286", "K842648", "K030721", "K961863", "K925216", "K890658", 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"device_class": "2" } } ] }