{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Chesapeake",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90650",
      "recalling_firm": "Family Dollar Stores, Llc.",
      "address_1": "500 Volvo Pkwy",
      "address_2": "",
      "postal_code": "23320-1604",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Product distributed to Family Dollar retail stores in US nationwide.",
      "recall_number": "Z-1541-2022",
      "product_description": "NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ, SKU 999417",
      "product_quantity": "28",
      "reason_for_recall": "Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.",
      "recall_initiation_date": "20220623",
      "center_classification_date": "20220817",
      "report_date": "20220824",
      "code_info": "All product sold between May 1, 2022 - June 10, 2022.",
      "more_code_info": ""
    }
  ]
}