{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Santa Maria",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97136",
      "recalling_firm": "Preat Corp",
      "address_1": "2625 Skyway Dr Ste B",
      "address_2": "N/A",
      "postal_code": "93455-1405",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, FL, GA, KY, MD, MN, NY, OK, PA.",
      "recall_number": "Z-2107-2025",
      "product_description": "Preat, Astra EV-compatible 4.2mm Digital Analog  REF: 9006603 (single) and 9006603-10(10 pack), Rx Only",
      "product_quantity": "44 units",
      "reason_for_recall": "Due to manufacturing error, digital analog rotational feature is 180 degrees off.",
      "recall_initiation_date": "20250624",
      "center_classification_date": "20250710",
      "report_date": "20250716",
      "code_info": "Lots: 278735, & 278402/UDI:",
      "more_code_info": ""
    }
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}