{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Road",
      "reason_for_recall": "Arrow International, Inc. is notifying customers that lot 23F13K0969 of product code ASK-05501-AFH1 contains an incorrect component. The lidstock indicates that the kit contains one \u001cSyringe, 10mL, Luer-Slip Loss of Resistance, Glass\u001d but contains one \u001cSyringe, 10mL, Luer-Lock Loss of Resistance, Glass.",
      "address_2": "",
      "product_quantity": "300",
      "code_info": "Catalog No. ASK-05501-AFH1        Lot Number 23F13K0969",
      "center_classification_date": "20141022",
      "distribution_pattern": "US Distribution in Utah only.",
      "state": "PA",
      "product_description": "ASK-05501-AFH1, Lot Number 23F13K0969 Anesthesia Conduction Catheter, Epidural Anesthesia Kit",
      "report_date": "20141029",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-0114-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69256",
      "termination_date": "20151218",
      "more_code_info": "",
      "recall_initiation_date": "20140915",
      "postal_code": "19605",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}