{
  "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": [
    {
      "country": "United States",
      "city": "Salisbury",
      "address_1": "9 Fanaras Dr",
      "reason_for_recall": "Incomplete packaging seal of sterile product",
      "address_2": "",
      "product_quantity": "8500 Cases",
      "code_info": "Manufacturer's product or Catalog # 5400S   Expiration Date: 01OCT2021-14JUN2022  Lot # CI0PVV, CI0V78, CI0X0B, CI16CG, CI17BB, CI18KB, CI18Y7, CI1E36, CI1JCE",
      "center_classification_date": "20191023",
      "distribution_pattern": "US Nationwide distribution including the states of MA, TX, RI, OH, NY, MN, SD, IL, MO, FL, VA, NE, UT, CA",
      "state": "MA",
      "product_description": "Sterile Co-Flex NL 4\" - Product Usage: Single Use secondary wound dressing or compression wrap",
      "report_date": "20191030",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Andover Healthcare Inc.",
      "recall_number": "Z-0180-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "83239",
      "termination_date": "20200909",
      "more_code_info": "",
      "recall_initiation_date": "20190619",
      "postal_code": "01952-1444",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}