{
  "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": [
    {
      "country": "United States",
      "city": "Keene",
      "address_1": "10 Bowman Dr",
      "reason_for_recall": "Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have broken luers.",
      "address_2": "",
      "product_quantity": "720,100 total devices",
      "code_info": "Portex LineDraw Arterial Blood Sampling Syringe:  Item Number              Lot Number  4042-2                   3848838  4042-2                   3848878  4042-2                   3856950  4042-2                   3859774  4042LH                   3856958  4042LH                   3859747",
      "center_classification_date": "20200415",
      "distribution_pattern": "USA:  AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI,MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA.    Int'l:  CA, DE, AU.",
      "state": "NH",
      "product_description": "Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin for Gases and Electrolytes",
      "report_date": "20200422",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smiths Medical ASD, Inc.",
      "recall_number": "Z-1715-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84681",
      "termination_date": "20201214",
      "more_code_info": "",
      "recall_initiation_date": "20200107",
      "postal_code": "03431-5043",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}