{
  "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": "Terminated",
      "city": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85104",
      "recalling_firm": "Maquet Cardiovascular Us Sales, Llc",
      "address_1": "45 Barbour Pond Dr",
      "address_2": "N/A",
      "postal_code": "07470-2094",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution only to the following states: AL  AZ  CA  CT  FL  GA  IL  MA  MI  NC  NH  NM  NY  OH  OK  TN  TX  VA",
      "recall_number": "Z-1603-2020",
      "product_description": "Avalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039",
      "product_quantity": "255",
      "reason_for_recall": "A lot of Avalon Elite Vascular Access Kits (VAK) are being recalled due to a material mix-up with the needle portion of the kit; 81 of 255 kits were assembled with an incorrect Arterial Access Needle instead of a  Multi-Purpose Procedure Needle.",
      "recall_initiation_date": "20200220",
      "center_classification_date": "20200327",
      "termination_date": "20220118",
      "report_date": "20200408",
      "code_info": "Lot 19-03466"
    }
  ]
}