{
  "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": "2026-04-01",
    "results": {
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    {
      "status": "Terminated",
      "city": "Glendora",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "72111",
      "recalling_firm": "Oasis Medical, Inc.",
      "address_1": "514 S Vermont Ave Bldg 510-528",
      "address_2": "N/A",
      "postal_code": "91741-6205",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "FL",
      "recall_number": "D-1418-2015",
      "product_description": "ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose), 1 Single Use Syringe, 0.07 fl oz (2mL), 1 Single Use Applicator Tip per carton, Manufactured for OCULUS SURGICAL, Port St. Lucie, FL 34986, NDC 62144-5510-05",
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      "reason_for_recall": "Falied pH specification",
      "recall_initiation_date": "20150831",
      "center_classification_date": "20150909",
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      "report_date": "20150916",
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