{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85287",
      "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": "AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX),",
      "recall_number": "Z-1946-2020",
      "product_description": "PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length  Catalog Number: ST018101D",
      "product_quantity": "655 kits",
      "reason_for_recall": "Iincorrectly packaged without the required lidocaine as labeled",
      "recall_initiation_date": "20200317",
      "center_classification_date": "20200508",
      "termination_date": "20201021",
      "report_date": "20200520",
      "code_info": "Lot Number: REDW0476 20  Exp. Date: 20OCT30  UDI: (01)00801741139390"
    }
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}