{
  "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": "San Diego",
      "address_1": "10020 Pacific Mesa Blvd",
      "reason_for_recall": "The recall was initiated because Carefusion identified a potential risk associated with the Alaris Pump module model 8100.  Carefusion has received reports of customers experiencing motor stalls during infusion with Alaris Pump Module (model 8100) manufactured between August 2010 and July 2011.",
      "address_2": "",
      "product_quantity": "102,248 units",
      "code_info": "All serial numbers associated with the Alaris Pump Module Model 8100: 8100 DEMO PUMP MODULE; 8100 Global Pump Module; 8100 IOC Pump Module V8.5.29.0; 8100 LVP Training Unit; 8100 Pump Module V8.5.29.0; 8100 Pump Module V8.5.29.0 (V9); Medley Patient Care System LVP; Model 8100 Trade-In Material; RCND 8100 Pump Module V8.5.29.0",
      "center_classification_date": "20120815",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and the countries of: South Africa and Canada.    Additional Countries:  Netherlands.",
      "state": "CA",
      "product_description": "Alaris Pump Module model 8100.    Subsequent product code: FPA    The Pump module is intended for facilities that utilize infusion for the delivery of fluids, medications, blood, and blood products using continuous or intermittent delivery through clinically acceptable routes of administration; such as, intravenous (IV), intra-arterial (IA),subcutaneous, epidural, enteral, or irrigation of fluid spaces. The Pump module is indicated for use on adults, pediatrics, and neonates.",
      "report_date": "20120822",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "CareFusion 303, Inc.",
      "recall_number": "Z-2185-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "55121",
      "termination_date": "20150826",
      "more_code_info": "",
      "recall_initiation_date": "20120629",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}