{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82245",
      "recalling_firm": "COVIDIEN LLC",
      "address_1": "15 Hampshire St",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  CA, NJ, and WA.",
      "recall_number": "Z-1041-2019",
      "product_description": "Kendall SCD Express Sterile Sleeves (Thigh Length), Model Number 9736",
      "product_quantity": "25 units",
      "reason_for_recall": "The product does not meet sterility requirements.  Product labeled as sterile was distributed without undergoing sterilization prior to distribution.",
      "recall_initiation_date": "20190215",
      "center_classification_date": "20190322",
      "termination_date": "20200724",
      "report_date": "20190403",
      "code_info": "Lot Number  83410S09D"
    }
  ]
}