{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tempe",
      "address_1": "1810 W Drake Dr",
      "reason_for_recall": "3040 compression sleeves being mislabeled as a 3010-PL compression sleeves.",
      "address_2": "",
      "product_quantity": "280 devices",
      "code_info": "Lot 6285035.    UDI: 00885825016661.",
      "center_classification_date": "20171221",
      "distribution_pattern": "Distributed to Texas.",
      "state": "AZ",
      "product_description": "3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector.    Intended for use in preventing deep vein thrombosis (DVT), diminishing post-operative pain and swelling, enhancing blood circulation and reducing wound healing time on the calf.",
      "report_date": "20171227",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Sustainability Solutions",
      "recall_number": "Z-0272-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "78714",
      "termination_date": "20180927",
      "more_code_info": "",
      "recall_initiation_date": "20171201",
      "postal_code": "85283-4327",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}