{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88531",
      "recalling_firm": "B. Braun Medical, Inc.",
      "address_1": "901 Marcon Blvd",
      "address_2": "N/A",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution and the country of Canada.",
      "recall_number": "Z-2547-2021",
      "product_description": "60 drops/ml, Priming volume: 25 ml, Length: 120 in.in-single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids  Ref:  354215",
      "product_quantity": "1,960 units",
      "reason_for_recall": "Leakage of the pump set within the cassette portion of the pump sets, potential for delays in administration of medications, under-delivery  or incomplete dosing and bloodstream infections.",
      "recall_initiation_date": "20210810",
      "center_classification_date": "20210924",
      "termination_date": "20240916",
      "report_date": "20211006",
      "code_info": "Lot Code: 0061758630 0061763934  DI: 04046964182259"
    }
  ]
}