{ "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": "203824", "product_res_number": "Z-0506-2024", "event_date_initiated": "2023-11-03", "event_date_posted": "2023-12-07", "recall_status": "Open, Classified", "res_event_number": "93277", "product_code": "IPF", "k_numbers": [ "K093138" ], "product_description": "Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation", "code_info": "UDI/DI 00860000178303, Serial Numbers: 181102627, 180101759, 180302368, 180603258, 180101748, 180603502, 160700386, 170305821, 170305701, 180603845, SZ151100022, 180603489, SZ160801811, 180603829, 151100395, 180101912, 181102643, 160800430, 180603799, 160800489, 181102635, 181102714, 180302357, 181102642, 161202284, 160800483, 180603914, 180101917, 161202293, 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"recalling_firm": "Liberty Medical Solutions, LLC", "address_1": "3653 Madaca Ln", "city": "Tampa", "state": "FL", "postal_code": "33618-2048", "additional_info_contact": "Mr Matthew Kay\n800-932-0147", "reason_for_recall": "The instruction manuals that were included with the Multi-Mode Stimulators distributed from 2018 to 2023 did not contain all of the appropriate warnings and contraindications.", "root_cause_description": "Error in labeling", "action": "Liberty Medical Solutions, LLC issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 11/03/2023 via US Mail. 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"Stimulator, Muscle, Powered", "medical_specialty_description": "Physical Medicine", "regulation_number": "890.5850", "device_class": "2" } } ] }