{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Powell",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99728",
      "recalling_firm": "DeRoyal Industries Inc",
      "address_1": "200 Debusk Ln",
      "address_2": "",
      "postal_code": "37849-4703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of LA,MO, MD, TN, UT.",
      "recall_number": "Z-3256-2026",
      "product_description": "REF: 81-030415  Myocardial Probe Non-Pyrogenic , 400 Series",
      "product_quantity": "7 cases, 140 units",
      "reason_for_recall": "Myocardial temperature probes contain an incorrect needle. Specifically, an 18mm needle was included instead of a 15mm needle.",
      "recall_initiation_date": "20260820",
      "center_classification_date": "20260922",
      "report_date": "20260930",
      "code_info": "DI: 00749756046077/Lot # 63426754",
      "more_code_info": ""
    }
  ]
}