{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Golden",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70294",
      "recalling_firm": "CME America, LLC",
      "address_1": "14998 W 6th Ave",
      "address_2": "",
      "postal_code": "80401-6587",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide Distribution - Nationwide Distribution and VA/military/govt consignees and the country of Canada.",
      "recall_number": "Z-1126-2015",
      "product_description": "BodyGuard 323 pump, models  100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS,   100-603XSA and 100-603XSAP",
      "product_quantity": "3,186",
      "reason_for_recall": "CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due to the potential for an over delivery.",
      "recall_initiation_date": "20150116",
      "center_classification_date": "20150219",
      "termination_date": "20170331",
      "report_date": "20150225",
      "code_info": "All product with USA36A4.4 version of software affected",
      "more_code_info": ""
    }
  ]
}