{
  "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": "Bethlehem",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95171",
      "recalling_firm": "B Braun Medical Inc",
      "address_1": "824 12th Ave",
      "address_2": "",
      "postal_code": "18018-3524",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-3177-2024",
      "product_description": "STREAMLINE LONG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis.    Model/Catalog Number: SL-2000M2095W",
      "product_quantity": "142336 units",
      "reason_for_recall": "Incomplete insertion of the patient connector of the  Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rinseback procedures. If the patient connector is not fully inserted into the Locksite, the internal septum may not open fully enough to prevent restrictions to flow. may cause delays in therapy while clinicians are forced to switch to retrograde flow method",
      "recall_initiation_date": "20240815",
      "center_classification_date": "20240919",
      "report_date": "20240925",
      "code_info": "UDI-DI 04046955348800; All Unexpired Lot Numbers",
      "more_code_info": ""
    }
  ]
}