{ "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": "2026-08-20", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "38088", "product_res_number": "Z-0770-05", "event_date_initiated": "2005-03-18", "event_date_posted": "2005-04-27", "recall_status": "Terminated", "event_date_terminated": "2005-10-17", "res_event_number": "31528", "product_code": "LRO", "product_description": "Medline Custom Anesthesia Super Circuit Adult 60 Unilimb Kit (non-sterile), reorder number DYNJAAF6267; the kit contains the Nexus Adult Unilimb Circuit - 60'', part 60010-1B, along with a 3 liter latex breathing bag, anesthesia tubing clip, suction catheter, adult anesthesia mask, suction canister, drawstring poly bag and poly bag; Made in USA by Medline Industries, Inc., Mundelein, IL 60060", "code_info": "reorder number DYNJAAF6267, lots 04LD1288, 04LD1865, 05CD0012, 05CD0467", "firm_fei_number": "3000717925", "recalling_firm": "Medline Industries, Inc.", "address_1": "1170 S Northpoint Blvd", "city": "Waukegan", "state": "IL", "postal_code": "60085-6757", "additional_info_contact": "Ms. Lara M. Simmons \n800-879-2791 Ext. 6072", "reason_for_recall": "The procedure packs contain anesthesia/breathing circuits being recalled by MMS Sales due to partial occlusion of the T-piece resulting in airway obstruction.", "root_cause_description": "Other", "action": "Recalled from the direct account hospitals via letter dated 3/18/05 and 3/23/05. The letters informed the accounts of the occlusion via copy of the MMS recall letter, and listed the Medline reorder number and lot numbers of the custom packs shipped to them, along with the MMS part number contained there in. The accounts were requested to examine their stocks for the affected codes and return them to Medline.", "product_quantity": "2,960 kits", "distribution_pattern": "California, Alabama, Minnesota, Florida and Indiana.", "openfda": { "k_number": [ "K930270", "K964011", "K041080", "K963715", "K970187", "K935858", "K931824", "K930700", "K963443", "K935686", "K920292", "K933137", "K023276", "K925214", "K936117", "K961863", "K885090", "K873973", "K895202", "K934028", "K871322", "K934428", "K952539", "K880961", "K920267", "K884093", "K914935", "K854292", "K931673", "K212258", "K945481", "K925216", "K931760", "K910365", "K874439", "K902888", "K871437", "K935740", "K932220", "K935483", "K934688", "K932221", "K030721", "K962826", "K874760", "K941846", "K882684", "K890726", "K926269", "K950574", "K931844", "K901856", "K951149", "K961683", "K965201", "K980137", "K953083", "K945160", "K932217", "K922648", "K854095", "K934030", "K922133", "K934029", "K871459", "K890098", "K931820", "K924468", 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