{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Breinigsville",
      "state": "PA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95093",
      "recalling_firm": "B Braun Medical Inc",
      "address_1": "200 Boulder Dr",
      "address_2": "",
      "postal_code": "18031-1532",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US distribution to AL, CA, GA, IL, MI, and TX.",
      "recall_number": "Z-2972-2024",
      "product_description": "Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U",
      "product_quantity": "14",
      "reason_for_recall": "Extension of previous recall RES 92978. Pumps have the potential for upstream occlusion sensor to cease proper function due to buildup of electrostatic charge during operation triggering false downstream and upstream occlusion alarms. Additional devices have been affected.",
      "recall_initiation_date": "20240807",
      "center_classification_date": "20240906",
      "report_date": "20240918",
      "code_info": "UDI-DI (GUDID) - 04046963716752  Serial Numbers 52226, 107529, 123259, 123815, 123843, 139003, 147678, 147721, 147725, 239018, 239165, 239231, 239279, 339337",
      "more_code_info": ""
    }
  ]
}