{
  "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": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Arrow is recalling additional lots that were identified as part of an active recall. Arrow is recalling the affected product due to the possibility that the catheter peel-away component hub tabs may prematurely detach when the practitioner begins to peel apart the sheath body from the catheter.",
      "address_2": "",
      "product_quantity": "9,037 units in the U.S. and 4,505 Internationally",
      "code_info": "Device Listing # D184260  Material # PL-01055",
      "center_classification_date": "20170707",
      "distribution_pattern": "Distributed to SC, AL, NJ, IN, MA, GA, CA, PA, AZ, VA , WA and Bangkok",
      "state": "PA",
      "product_description": "Arrow Glide Thru Peel-Away Sheath/Dilator Introducer",
      "report_date": "20170719",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-2699-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77604",
      "termination_date": "20180906",
      "more_code_info": "",
      "recall_initiation_date": "20170612",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}