{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
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      "city": "Marietta",
      "state": "GA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98429",
      "recalling_firm": "Erbe USA Inc",
      "address_1": "2225 Northwest Pkwy SE",
      "address_2": "",
      "postal_code": "30067-8764",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-1567-2026",
      "product_description": "Flexible Cryoprobe (OD 1.7mm, L1.15mm)  REF: 20402-410. For surgical use",
      "product_quantity": "8,284 units",
      "reason_for_recall": "Probes may rupture/burst during activation",
      "recall_initiation_date": "20260212",
      "center_classification_date": "20260320",
      "report_date": "20260401",
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