{ "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": "2026-09-05", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "218618", "product_res_number": "Z-1474-2026", "event_date_initiated": "2026-02-05", "event_date_posted": "2026-02-26", "recall_status": "Open, Classified", "res_event_number": "98403", "product_code": "JSJ", "product_description": "Campy CVA Medium 100/PK, R01272", "code_info": "UDI-DI 848838001055\nLot R01272 lot 339135\nExpired January 12, 2026", "firm_fei_number": "1924669", "recalling_firm": "Remel, Inc", "address_1": "12076 Santa Fe Trail Dr", "city": "Lenexa", "state": "KS", "postal_code": "66215-3519", "additional_info_contact": "Erica Knox\n800-255-6730", "reason_for_recall": "Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.", "root_cause_description": "Under Investigation by firm", "action": "On February 5, 2026, the firm notified affected customers via Urgent Medical Device Recall letter. 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