{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lancaster",
      "address_1": "6 Lancaster Pkwy",
      "reason_for_recall": "Contact lenses lack sterility assurance.",
      "address_2": "",
      "product_quantity": "4",
      "code_info": "AZ128410",
      "center_classification_date": "20180313",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states:of CA, FL, GA, ID, IL, IN, KS, KY, MD, MI, MO, MS, NC, NJ, NM, NV, NY, OH, OR, PA, TX, VA, WI, WY and the country of Canada.",
      "state": "NY",
      "product_description": "ASTERA Multifocal Toric Daily Wear Soft contact; Catalog Number: AOAMT54    Product Usage:  The ALDEN TORIC LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia) and/or possesses refractive astigmatism not exceeding 10 Diopters.",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alden Optical",
      "recall_number": "Z-0991-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "79377",
      "termination_date": "20180619",
      "more_code_info": "",
      "recall_initiation_date": "20171103",
      "postal_code": "14086-9713",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}