{
  "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": "2026-04-22",
    "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": "80378",
      "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": "Puerto Rico",
      "recall_number": "Z-2576-2018",
      "product_description": "Percutaneous Sheath Introducer Kit for use with 7 -  7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia. spring-wire guide), REF ES-09807.  The percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.",
      "product_quantity": "60 units",
      "reason_for_recall": "Product contains dry natural rubber latex.  Label states Latex Free.",
      "recall_initiation_date": "20180523",
      "center_classification_date": "20180730",
      "termination_date": "20200520",
      "report_date": "20180808",
      "code_info": "Lot/Batch Number: 13F18A0037  Expiration Date/Expected Life: Apr 2019"
    }
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}