{
  "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": "2026-03-18",
    "results": {
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    {
      "status": "Ongoing",
      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92913",
      "recalling_firm": "B. Braun Medical, Inc.",
      "address_1": "901 Marcon Blvd",
      "address_2": "",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distributions to states of - AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA, TX, WA",
      "recall_number": "Z-2627-2023",
      "product_description": "Perifix¿ / Epidural anesthesia set, medicated",
      "product_quantity": "3440 units",
      "reason_for_recall": "Product may be mislabeled with an incorrect lid stock label.",
      "recall_initiation_date": "20230731",
      "center_classification_date": "20230921",
      "report_date": "20230927",
      "code_info": "UDI-DI: 04046964178726  Product Code: 332250; Lot Number 0061863524, expiration date 30.APR.2025",
      "more_code_info": ""
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}