{
  "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": "2026-09-17",
    "results": {
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      "cfres_id": "215830",
      "product_res_number": "Z-2606-2025",
      "event_date_initiated": "2025-08-22",
      "event_date_posted": "2025-09-19",
      "recall_status": "Open, Classified",
      "res_event_number": "97515",
      "product_code": "MVN",
      "k_numbers": [
        "K131378",
        "K190965",
        "K220070"
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      "product_description": "MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric.\n\n54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged.",
      "code_info": "Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898",
      "firm_fei_number": "3005724763",
      "recalling_firm": "CooperVision, Inc.",
      "address_1": "180 Thruway Park Dr",
      "city": "West Henrietta",
      "state": "NY",
      "postal_code": "14586-9798",
      "additional_info_contact": "Annette Nelson\n1-925-6604471",
      "reason_for_recall": "One lot manufactured with an invalid sterilization cycle.",
      "root_cause_description": "Under Investigation by firm",
      "action": "CooperVision contacted consignees via telephone call and letter on 08/27/2025.  Consignees were instructed to examine inventory and quarantine affected lot numbers, cease further distribution of product, and notify customers/patients if further distributed. Consignees were also requested to complete and return the Correction Response Form and arrange for the return of affected units.",
      "product_quantity": "4,140 units",
      "distribution_pattern": "US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.",
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        "device_name": "Lens, Contact, (Disposable)",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.5925",
        "device_class": "2"
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}