{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Monroe",
      "state": "LA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71569",
      "recalling_firm": "Gardner Denver Thomas Inc",
      "address_1": "4601 Central Ave",
      "address_2": "N/A",
      "postal_code": "71203-6003",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Internationally Distributed in the countries of :Mexico, Peru, El Salvador, Chile, Colombia, Vietnam, and Malaysia.",
      "recall_number": "Z-2151-2015",
      "product_description": "THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1243    Product Usage:  medical aspirator",
      "product_quantity": "508 units",
      "reason_for_recall": "Vacuum pump may not perform to specification.",
      "recall_initiation_date": "20150604",
      "center_classification_date": "20150720",
      "termination_date": "20160809",
      "report_date": "20150729",
      "code_info": "Serial numbers 2122-2629"
    }
  ]
}