{
  "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": "79200",
      "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": "AZ, CA, GA, MA, MO, NY, VA",
      "recall_number": "Z-0690-2018",
      "product_description": "ARROW¿ PICC  powered by ARROW¿ VPS¿  Stylet",
      "product_quantity": "601 eaches",
      "reason_for_recall": "The kit may contain an incorrect catheter component. Kits that should  contain a 40cm catheter may contain a 55cm catheter.",
      "recall_initiation_date": "20171017",
      "center_classification_date": "20180222",
      "termination_date": "20200421",
      "report_date": "20180228",
      "code_info": "CDC 34041 VPS  Lot# 23F17A0037  23F17B0035"
    }
  ]
}