{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Burnsville",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92247",
      "recalling_firm": "Apothecary Products, LLC",
      "address_1": "11750 12th Ave S",
      "address_2": "N/A",
      "postal_code": "55337-1297",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, HI, IL, IN, MO, NC, NJ, NY, OK, OR, PA, TN, TX, UT, WA and the country of Canada.",
      "recall_number": "Z-1703-2023",
      "product_description": "Medicine Dropper, Product Code K508",
      "product_quantity": "1,596 units",
      "reason_for_recall": "Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.",
      "recall_initiation_date": "20230330",
      "center_classification_date": "20230609",
      "report_date": "20230621",
      "code_info": "Lot Number: 021623; UPC Number: 077602005085"
    }
  ]
}