{
  "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": [
    {
      "country": "United States",
      "city": "Round Lake",
      "address_1": "Rt. 120 & Wilson Rd",
      "reason_for_recall": "After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX) control module, the AUTOMIX may generate an incorrect device response to an AUTOMIX operator's key press.  Also, the AUTOMIX system may experience an intermittent electrical failure, in which unexpected pump motor operations will occur. Also, the AUTOMIX system may intermittently experience an electrical failure where the  compounder may stop compounding without an alarm and not be detected by the user.",
      "address_2": "",
      "product_quantity": "840 units",
      "code_info": "Product code 2M8075, all serial numbers",
      "center_classification_date": "20120808",
      "distribution_pattern": "Worldwide Distribution - USA - Nationwide including Puerto Rico, and internationally to Brazil, Canada, Colombia, Costa Rica, Czech Republic, El Salvador, Egypt, Germany, Guatemala, Honduras, Luxembourg, Mexico, Panama, Saudi Arabia, Singapore, Switzerland, Taiwan, Trinidad, Turkey, United Arab Emirates and United Kingdom.",
      "state": "IL",
      "product_description": "AUTOMIX Plus High Speed Compounder System, product 2M8075; automated nutrition compounders;     Product Usage:  The Automix Compounder Systems are electromechanical positive displacement fluid compounding devices used in the admixture of large volume parenteral nutrition formulations via gravimetric weighing.",
      "report_date": "20120815",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corp.",
      "recall_number": "Z-2140-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62558",
      "termination_date": "20170811",
      "more_code_info": "",
      "recall_initiation_date": "20120713",
      "postal_code": "60073",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}