{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Allentown",
      "address_1": "901 Marcon Blvd",
      "reason_for_recall": "Potential for the Infusion Pump Administration Set to leak and/or disconnect at the bonded joint between the tubing and Injection Site (Y-Site).",
      "address_2": "",
      "product_quantity": "2580",
      "code_info": "Lot Number 0061641410",
      "center_classification_date": "20190923",
      "distribution_pattern": "Distribution to US state of TX, and Canada.",
      "state": "PA",
      "product_description": "B.Braun Infusomat Space Volumetric Infusion Pump Administration Set, Catalog Number 363032",
      "report_date": "20191002",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "B. Braun Medical, Inc.",
      "recall_number": "Z-2489-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82966",
      "termination_date": "20200713",
      "more_code_info": "",
      "recall_initiation_date": "20190501",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}