{
  "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": "Mocksville",
      "state": "NC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63347",
      "recalling_firm": "Ventlab Corporation",
      "address_1": "155 Boyce Dr",
      "address_2": "N/A",
      "postal_code": "27028-4187",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including IL, OH, NY and TN.",
      "recall_number": "Z-0176-2013",
      "product_description": "Safe Spot Infant Resuscitator, Pro-1900 Series, Single Patient Use,      The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.",
      "product_quantity": "14,602 total for all units",
      "reason_for_recall": "Possible volume leakage through the inlet valve during compressions of the resuscitator bag.",
      "recall_initiation_date": "20120711",
      "center_classification_date": "20121101",
      "termination_date": "20130630",
      "report_date": "20121107",
      "code_info": "Product List 071012, Product Codes: PRO-1904, Lot #100155, 100183, 100451, 100497, 100655, 101577 and PRO-1925, Lot #101550, 101604101657.",
      "more_code_info": ""
    }
  ]
}