{
  "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": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81375",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution.",
      "recall_number": "Z-0956-2019",
      "product_description": "AF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB, Product code MVBX60XL CPNB, Arrow AutoFuser Disposable Pain Control Pump",
      "product_quantity": "1",
      "reason_for_recall": "Possible cracks on the body of the fill port connector, which may result in a leak. If the leak is identified while the user is filling the pump, there may be a delay  while an alternative pump is located. If the leak goes undetected it may result in a reduced level of drug  delivery to the patient and consequently a lower level of pain relief than that prescribed or expected. This  may result in the need for other, additional analgesic drug administration.",
      "recall_initiation_date": "20181002",
      "center_classification_date": "20190225",
      "termination_date": "20211112",
      "report_date": "20190306",
      "code_info": "74E1702443",
      "more_code_info": ""
    }
  ]
}