{
  "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": "5",
      "code_info": "AZ162110  AZ162120  AZ158510  AZ158520  AZ160420",
      "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": "Alden HP59 Toric Daily Wear Soft contact; Catalog Number: AOHPT59    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-0990-2018",
      "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"
    }
  ]
}