{ "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": "2026-08-13", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "49045", "product_res_number": "Z-0211-2007", "event_date_initiated": "2006-10-27", "event_date_posted": "2006-11-22", "recall_status": "Terminated", "event_date_terminated": "2012-05-22", "res_event_number": "36643", "product_code": "CAZ", "k_numbers": [ "K965017" ], "product_description": "Portex Continuous Epidural tray \nRef 4948-17", "code_info": "Lot Number: 1063342", "firm_fei_number": "1217052", "recalling_firm": "Smiths Medical ASD, Inc.", "address_1": "10 Bowman Dr", "city": "Keene", "state": "NH", "postal_code": "03431-5043", "additional_info_contact": "Timothy J. Talcott\n603-352-3812 Ext. 2457", "reason_for_recall": "Misbranded: Tray label states 26G x 5/8 inch, needle is 25 G x 1 inch", "root_cause_description": "Other", "action": "Smith Medical notified Dealers and direct customers contacted via letter delivered by Federal Express on October 27, 2006. 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