{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
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      "city": "Saint Paul",
      "state": "MN",
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      "classification": "Class II",
      "openfda": {},
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      "event_id": "78419",
      "recalling_firm": "Ecolab, Inc.",
      "address_1": "940 Lone Oak Rd",
      "address_2": "N/A",
      "postal_code": "55121-2214",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed domestically to Michigan.",
      "recall_number": "Z-0523-2018",
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      "product_quantity": "5,958 cases (50 per case)",
      "reason_for_recall": "Sterile packaging of the disposable light handle cover may contain gaps in the seal of the pouch.",
      "recall_initiation_date": "20171013",
      "center_classification_date": "20180205",
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