{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Product lidstock contains the incorrect expiration date for the product",
      "address_2": "",
      "product_quantity": "870",
      "code_info": "Lot Number:   13F18A0451",
      "center_classification_date": "20200214",
      "distribution_pattern": "Nationwide  Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA",
      "state": "PA",
      "product_description": "Arrow¿ EPIDURAL CATHETERIZATION KIT  AK-05000",
      "report_date": "20200226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-1245-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84688",
      "termination_date": "20210225",
      "more_code_info": "",
      "recall_initiation_date": "20191220",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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  ]
}