{
  "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": "Kansas City",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90574",
      "recalling_firm": "American Contract Systems, Inc.",
      "address_1": "2610 Ne Industrial Dr Ste 220",
      "address_2": "N/A",
      "postal_code": "64117-2648",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distribution within the United States to health systems and distributors in AZ, FL, IA, IL, MA, MN, MO, OH, NE, PA, RI, SD, and TX",
      "recall_number": "Z-1697-2022",
      "product_description": "Breast Abdominoplasty Pack",
      "product_quantity": "1 unit",
      "reason_for_recall": "Product was exposed to multiple sterilization cycles without validation for multiple exposures.",
      "recall_initiation_date": "20220616",
      "center_classification_date": "20220908",
      "report_date": "20220914",
      "code_info": "Tray Number, Sterilization Lot, Lot Number, Bag Serial Number   1) SWBA26F, 2106091, 842211, 64133051-006"
    }
  ]
}