{
  "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": "2026-09-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "222436",
      "product_res_number": "Z-3248-2026",
      "event_date_initiated": "2026-08-12",
      "event_date_posted": "2026-09-18",
      "recall_status": "Open, Classified",
      "res_event_number": "99766",
      "product_code": "MVN",
      "k_numbers": [
        "K130331"
      ],
      "product_description": "Brand Name: Pearle Vision 1 day\nProduct Name: (somofilcon A) Contact Lens\nModel/Catalog Number: Pearle Vision 1 day",
      "code_info": "Pearle Vision 1 day;\n\nCarton Lot # 11727620152030;\nBlister Lot # CB132348;",
      "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\n585-756-9300",
      "reason_for_recall": "A small number of lenses within the affected lot are of the incorrect power.",
      "root_cause_description": "Process control",
      "action": "On August 24, 2026 URGENT MEDICAL DEVICE CORRECTION letters were sent to customers. \nActions to be taken:\n1. Please stop any further distribution of products from the designated lot number.\n2. Dispose of the affected product in your inventory or that is returned to you.\n3. Within the next five (5) business days, please complete the response form provided and return it. If you have no lenses from these specified lots, please put  0  in  Quantity  and return the form.\n4. We recommend authorized distributors contact your accounts, and Eye Care Practitioners contact your patients who have received the affected product, with the enclosed  Customer Communication Letter .\n5. Please instruct any patients to return any affected product to their Eye Care Practitioner or purchase location for replacement or credit.",
      "product_quantity": "3060",
      "distribution_pattern": "US Nationwide distribution in the states of MN, OH, WI.",
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        "device_name": "Lens, Contact, (Disposable)",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.5925",
        "device_class": "2"
      }
    }
  ]
}