{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Branford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82971",
      "recalling_firm": "Madison Polymeric Engineering",
      "address_1": "965 W Main St",
      "address_2": "N/A",
      "postal_code": "06405-3453",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  AZ, CA, FL, IA, IL, IN, MA, MD, MO, PA, TN, TX, WA.",
      "recall_number": "Z-1925-2019",
      "product_description": "First Step Draco Pad, Product Number EP-4D",
      "product_quantity": "10570",
      "reason_for_recall": "This product has been contaminated with Stenotrophomonas lactiubi.",
      "recall_initiation_date": "20190508",
      "center_classification_date": "20190702",
      "termination_date": "20200706",
      "report_date": "20190710",
      "code_info": "Lot Numbers EX20191221X  EX20191226X  EX20191227X  EX20191228X"
    }
  ]
}