{
  "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": {
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  "results": [
    {
      "cfres_id": "220034",
      "product_res_number": "Z-2260-2026",
      "event_date_initiated": "2026-04-10",
      "event_date_posted": "2026-05-28",
      "recall_status": "Open, Classified",
      "res_event_number": "98866",
      "product_code": "OJK",
      "product_description": "Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P",
      "code_info": "UDI/DI 10198459151569 (each), 40198459151560 (case), Lot Numbers:  26BMC538",
      "firm_fei_number": "1417592",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "city": "Northfield",
      "state": "IL",
      "postal_code": "60093-2753",
      "additional_info_contact": "Haley Barclay\n866-359-1704",
      "reason_for_recall": "Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and blister pack are labeled as a 1 mL Luer Lock Tuberculin Syringe (Product Code 1180100777), but the syringes inside are U-100 insulin syringes.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Medline Industries, LP issued an URGENT MEDICAL DEVICE RECALL notice to it consignees on 4/10/2026 via USPS first class mail and email.  The notice explained the issue, potential risk, and requested the following:  \n\"REQUIRED ACTION:\n1. Immediately check your stock for the affected item number(s) and the affected lot number(s) listed on the enclosed response form. Quarantine all affected product.\n2. Please complete and return the enclosed response form listing the quantity of affected product you have in inventory. Even if you do not have any affected product in inventory, please complete and return the response form.\n3. Upon receipt of your submitted response form, your account will receive over-labels to place on affected inventory, with instructions for your staff to remove and discard the affected component prior to using the kit. These labels will be provided via FedEx overnight, if applicable.\n4. If you are a distributor or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please include your customers  quantities on your response form. Upon receipt of your submitted response form, you will receive over-labels to provide to your customers to affix to their affected product.\"  \nFor questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.",
      "product_quantity": "8 kits",
      "distribution_pattern": "US Nationwide distribution in the states of California.",
      "openfda": {
        "device_name": "Eye Tray",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.4790",
        "device_class": "2",
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