{
  "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 II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94637",
      "recalling_firm": "B Braun Medical Inc",
      "address_1": "200 Boulder Dr",
      "address_2": "N/A",
      "postal_code": "18031-1532",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Canada.",
      "recall_number": "Z-2133-2024",
      "product_description": "Stimuplex A, 30 DEG, 20GX6\", 0.90x150mm, Catalogue Number: 4894278",
      "product_quantity": "108,811 units",
      "reason_for_recall": "The devices are labeled \"not made with DEHP\" or the DEHP free symbol; however, the glue used contains traces of DEHP.",
      "recall_initiation_date": "20240517",
      "center_classification_date": "20240611",
      "report_date": "20240619",
      "code_info": "Catalogue Number: 4894278; UDI/DI: 04022495101266; Lot/Batch: 20E15, 21E18, 19F08, 19G10, 19G13, 19G19, 19I19, 20C28, 20C31, 20D10, 20L19, 21B13, 21I17, 21K21, 21L12, 21M16, 22D12, 22H20, 22I22, 22K27, 23A20, 23C04, 23D14, 23F09, 23I08, 23I29,"
    }
  ]
}