{
  "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": "Ongoing",
      "city": "Greensboro",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82039",
      "recalling_firm": "ConvaTec, Inc",
      "address_1": "7900 Triad Center Dr Ste 400",
      "address_2": "N/A",
      "postal_code": "27409-9076",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of IL, MI, PA, WI.  and the countries of Algeria, Australia, Austria, Belgium, Canada, Croatia, Czechia, Czech Republic, Denmark, Egypt, Estonia, Finland, Faroe Islands, France, Germany, Greece, Hong Kong, Hungary, Iceland, Israel, Italy, Kenya, Korea, Kuwait, Lebanon, Myanmar, Netherlands, New Zealand, Norway, Poland, Qatar, Singapore, Spain, Slovakia, South Africa, Sweden, Switzerland, Turkey, United Arab Emirates, United Kingdom, United States, Vietnam.",
      "recall_number": "Z-1038-2019",
      "product_description": "FilterFlow Suction Handle CH24, 20 eaches per sales unit.    Product Usage:  Filter Flow is designed for orthopedic surgery and combines suctioning function with filtering. The device is intended for orthopedic surgical procedures to remove and collect debris and bone fragments, chips, cement, marrow and blood clots without blocking the suction device, using a combination of suctioning and filtering.",
      "product_quantity": "124,000 units total",
      "reason_for_recall": "An internal assessment of packaging confirmed the potential for a breach in the sterile barrier.",
      "recall_initiation_date": "20190109",
      "center_classification_date": "20190321",
      "report_date": "20190327",
      "code_info": "Product Code/REF Number: 504159; Lot Codes: 176482, 189027"
    }
  ]
}