{
  "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": "Terminated",
      "city": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82070",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "N/A",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL, NC",
      "recall_number": "Z-1118-2019",
      "product_description": "Arrow¿ Two-Lumen Central Venous Catheterization  Kit with Blue FlexTip¿ Catheter  Product Code: AH-11802  (OUS)  GTN: 00801902026132",
      "product_quantity": "None (US)",
      "reason_for_recall": "The product lidstock contains a labelling error. The lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct",
      "recall_initiation_date": "20190110",
      "center_classification_date": "20190410",
      "termination_date": "20200604",
      "report_date": "20190417",
      "code_info": "Lot Numbers:   71F14E0696 71F14K0658 71F15E0493 71F15L0621  71F14E1541 71F14K1683 71F15F0090 71F15M0787  71F14F1154 71F14L0719 71F15H0574 71F16A0278  71F14H0474 71F14M1375 71F15H1503 71F16B0054  71F14H1215 71F15A0025 71F15J0570 71F16B1306  71F14J0852 71F15A1592 71F15J2098  71F14J1889 71F15D1460 71F15L0153"
    }
  ]
}