{ "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": "47149", "product_res_number": "Z-0202-2007", "event_date_initiated": "2006-03-10", "event_date_posted": "2006-11-22", "recall_status": "Terminated", "event_date_terminated": "2008-04-24", "res_event_number": "35920", "product_code": "IPS", "product_description": "Access Point Medical Canes, Cane, Off-Set Crook w/Strap-Black, Product Code CN10051, packaged 20/case. The responsible firm is Access Point Medical, St. Louis, MO.", "code_info": "All canes bearing the model number.", "firm_fei_number": "3005009085", "recalling_firm": "Access Point Medical LLC", "address_1": "Three City Place Drive", "address_2": "Suite 750", "city": "St. Louis", "state": "MO", "postal_code": "63141", "additional_info_contact": "Richard A. Davis\n314-255-2702", "reason_for_recall": "The canes were made of unacceptable materials and could break", "root_cause_description": "Other", "action": "The firm began making telephone calls and issuing recall letters dated 3/9/06 via UPS on 3/10/06. The telephone call explained the reason for recall and notified the customer they would be receiving a letter requesting return of the canes. The letter additionally notified the customer the recall was to be affected to the retail level. A customer response form was enclosed.\n\nThe firm issued a second recall letter dated 12/22/06 via registered mail on 12/26/06 explaining the reason for recall, pointing out the hazard involved with the use of the recalled canes, and requesting they cease sales of the product. The letter requested they notify their customers of the recall and to post the enclosed recall placard where it can be seen by returning customers. Recall instructions were enclosed outlining step-by-step instructions for their customer to follow, including destroying the canes on site. A Customer Response Form was also enclosed.\n\nThe firm issued a third letter dated 1/11/07 via regular mail which included a corrected placard because the product code numbers were incorrect in the placard included with the letter dated 12/22/06. The customers were instructed to discard the previous placard.", "product_quantity": "78/20-cane cases", "distribution_pattern": "Nationwide.", "openfda": { "k_number": [ "K832970", "K772267", "K790558", "K832969", "K790561", "K790299", "K821402", "K770529", "K780085" ], "registration_number": [ "3010101089", "3004859140", "3010694026", "3005271071", "3038772401", "3015772781", "3008146511", "1043646", "3014690514", "3006984916", "3012327277", "3004905643", "2648727", "3043479340", "3043105505", "3019502344", "1000252066", "3009425497", "3006147977", "3017638267", "3009683397", "3016734231", "3012444100", "3008997160", "3013875443", "3034731542", "1422443", "3008386649", "3011669224", "3033849261", "3006897028", "3011191255", "3016159374", "3015214304", "3010603176", "3004111085", "3003781173", "3015924896", "3007518294", "3015277818", "9680333", "3017538926", "3031082325", "1523547", "3009703496", "3009567010", "3004361304", "3013495708", "3003775119", "3011659676", "3007499787", 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"medical_specialty_description": "Physical Medicine", "regulation_number": "890.3075", "device_class": "1" } } ] }