{ "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": "114924", "product_res_number": "Z-0171-2014", "event_date_initiated": "2012-11-29", "event_date_posted": "2013-11-06", "recall_status": "Terminated", "event_date_terminated": "2014-12-08", "res_event_number": "63859", "product_code": "FSA", "product_description": "Handset component of the Handicare USA's Minivator Bath Bliss Reclining Bath Lifts (Bath Bliss), Part Number BP300-100/BP300-400RSUS (handset) - Model Numbers BBR0311USAB (blue) and BBR0311USSS (silver)\r\n\r\nHandset component devices operate the Minivator Bath Bliss Reclining Bath Lift, a non-AC-powered patient lift consisting of a motorized actuator, powered mechanical seating device, temporarily secured in a bath, and used to lift and lower a patient in the vertical or reclining position while bathing.", "code_info": "Handsets shipped with Bath Lifts belonging to the following serial numbers: BH05100001 - BH05129999 and BH06120001 - BH11129999; Handsets shipped as spare parts with the following serial numbers: BS05100001 - BS05129999 and BS06120001 - BS11129999.", "firm_fei_number": "3007802293", "recalling_firm": "Handicare Accessibility", "address_1": "2201 Hangar Place", "address_2": "#200", "city": "Allentown", "state": "PA", "postal_code": "18109", "reason_for_recall": "Firm became aware that two handsets in the affected batches became inoperable while the user was in the tub.", "root_cause_description": "Device Design", "action": "Handicare sent an Urgent Medical Device Recall letter dated November 29, 2012, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to immediately advise all of their customers affected by the recall letter to immediately remove all affected product from use. Upon receipt of affected product, replacement handsets would be sent to customers. Customers with questions were instructed to call 866-276-5438 or email Customerservice.usa@handicare.com. \r\nFor questions regarding this recall call 610-266-5260.", "product_quantity": "3301 handsets", "distribution_pattern": "Worldwide distribution: USA (Nationwide) and country of: Canada.", "openfda": { "k_number": [ "K851844", "K860837", "K942807", "K823206", "K841395", "K840997", "K930625", "K811899", "K902141", "K780684", "K792601", "K844976", "K841398" ], "registration_number": [ "3007608806", "3007031002", "3010880685", "3009327812", "3005748481", "2132280", "3036834029", "3007689746", "3039527731", "3005484027", "8022890", "3024761165", "3003775119", "3021599329", "3004648937", "1417592", "3007309299", "3009425497", "3008406502", "3007518069", "3034694766", "3010472212", "3007802293", "3014523858", "1000211739", "3010398927", "3007420694", "3038008630", "3008555994", "3018050094", "1225263", "3004615451", "3017264244", "3008485769", "3016678950", "3007539307", "1041130", 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