{
  "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": "2026-09-10",
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      "event_date_initiated": "2022-05-11",
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      "recall_status": "Open, Classified",
      "res_event_number": "90196",
      "product_code": "OHY",
      "product_description": "Medline Pill Splitters; 1 each/box; 144 boxes/carton",
      "code_info": "Model Number: NON135000; UDI/DI:8019673489; Lot Numbers: 50920060001, 50920080001, 50920110001, 50921030001, 50921040001, 50921050001, 50921060001, 50921080001, 50921090001, 50921100001, 50921110001, 50921120001, 50922020001",
      "firm_fei_number": "1417592",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "city": "Northfield",
      "state": "IL",
      "postal_code": "60093-2753",
      "additional_info_contact": "Karin Johnson\n224-931-1071",
      "reason_for_recall": "Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.",
      "root_cause_description": "Process change control",
      "action": "The firm issued a recall notice to consignees on 05/11/2022 via mail. The letter instructs the consignee to check their stock, destroy affected product, and return the response form. On 5/16/2022, the firm sent out an updated recall notice.",
      "product_quantity": "840,087 each",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Singapore, Panama, and Hongkong.",
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