{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Salem",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73734",
      "recalling_firm": "American Surgical Company",
      "address_1": "45 Congress St",
      "address_2": "N/A",
      "postal_code": "01970-5579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the countries of Australia, Belgium, Canada, France, Germany, Greece, Hong Kong, Hong Kong, Israel, Italy, Italy, Japan, Netherlands, New Zealand, Portugal, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom.",
      "recall_number": "Z-1721-2016",
      "product_description": "American Surgical Delicot 15mm x 20mm  Ref: 63-04  Product Usage:  Neurosurgical and Nonneurosurgical Sponges",
      "product_quantity": "351 boxes",
      "reason_for_recall": "Product packaging defective compromising sterility",
      "recall_initiation_date": "20160331",
      "center_classification_date": "20160526",
      "termination_date": "20161021",
      "report_date": "20160601",
      "code_info": "Lot Number:/  2015/08 BH  2015/09 BP  2015/10 BM  2015/11 BL  2015/12 AX  2015/12 CR  2016/01 AN"
    }
  ]
}