{
  "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": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85334",
      "recalling_firm": "Becton Dickinson & Company",
      "address_1": "1 Becton Dr",
      "address_2": "N/A",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states: IN, MO, OH, and TX.",
      "recall_number": "Z-2078-2020",
      "product_description": "BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000277",
      "product_quantity": "1262 total",
      "reason_for_recall": "The kits contain surgical gowns which were subject to a recall by the supplier.",
      "recall_initiation_date": "20200226",
      "center_classification_date": "20200521",
      "termination_date": "20200922",
      "report_date": "20200527",
      "code_info": "Lot Numbers: 18PB2134  19FBP619"
    }
  ]
}