{
  "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-2268-2026",
      "product_description": "Brand Name: B. BRAUN MEDICAL INC.  Product Name: CESK RIVERSIDE HEALTH SYSTEM  Model/Catalog Number: 552126  Software Version: N/A  Product Description: CESK RIVERSIDE HEALTH SYSTEM  Component: No",
      "product_quantity": "690",
      "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 552126, UDI-DI (Primary Device) 04046955056903, UDI-DI (Unit Device ID) 04046955056897, Lot Number 0062031274",
      "more_code_info": ""
    }
  ]
}