{
  "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": "2026-06-24",
    "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": "98862",
      "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 in the states of AL, FL, PA, TX, VA, WA.",
      "recall_number": "Z-2267-2026",
      "product_description": "Brand Name: B. BRAUN MEDICAL INC.  Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID  Model/Catalog Number: 530184  Software Version: N/A  Product Description: LYNDON B JOHNSON HOSPITAL SPINAL EPID  Component: No",
      "product_quantity": "620",
      "reason_for_recall": "B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of  MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.",
      "recall_initiation_date": "20260129",
      "center_classification_date": "20260529",
      "report_date": "20260610",
      "code_info": "Lot Code: Model No 530184, UDI-DI (Primary Device) 04046955156528, UDI-DI (Unit Device ID) 04046955156511, Lot Number 0062019858",
      "more_code_info": ""
    }
  ]
}