{
  "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": "Ongoing",
      "city": "Vista",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82967",
      "recalling_firm": "DJO, LLC",
      "address_1": "1430 Decision St",
      "address_2": "N/A",
      "postal_code": "92081-8553",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed domestically, Oklahoma",
      "recall_number": "Z-1985-2019",
      "product_description": "Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003,  Expiration Date: 2020 -12 - 31, Made in Mexico, DJO, LLC.",
      "product_quantity": "9 units",
      "reason_for_recall": "The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.",
      "recall_initiation_date": "20190117",
      "center_classification_date": "20190718",
      "report_date": "20190724",
      "code_info": "Lot # 418003 UDI: (01)00888912302418"
    }
  ]
}