{
  "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": "2026-07-08",
    "results": {
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  "results": [
    {
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      "city": "Richmond",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        "is_original_packager": [
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        "unii": [
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      "product_type": "Drugs",
      "event_id": "90553",
      "recalling_firm": "Mckesson Medical-Surgical Inc. Corporate Office",
      "address_1": "9954 Maryland Drive",
      "address_2": "Deep Run Iii Ste. 4000",
      "postal_code": "23233",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "Nationwide in the USA.",
      "recall_number": "D-1321-2022",
      "product_description": "Pataday, Once Daily Relief, Olopatadine hydrochloride ophthalmic solution 0.2%, Antihistamine, Eye Allergy Itch Relief, Once Daily, Sterile, 2.5 mL (0.085 FL OZ) bottle per box, Alcon, NDC 0065-8150-01.",
      "product_quantity": "1 box",
      "reason_for_recall": "CGMP Deviations: products were stored outside the drug label specifications.",
      "recall_initiation_date": "20220629",
      "center_classification_date": "20220805",
      "termination_date": "20240213",
      "report_date": "20220817",
      "code_info": "Part# 00065815001",
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}