{
  "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": "2026-09-23",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Indianola",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99698",
      "recalling_firm": "Bayer Medical Care, Inc.",
      "address_1": "1 Bayer Dr",
      "address_2": "N/A",
      "postal_code": "15051-9702",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-3147-2026",
      "product_description": "MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System;  Catalog number: FLEXS-150-QFT;",
      "product_quantity": "27800 kits (556 boxes)",
      "reason_for_recall": "Some devices may not have been properly sterilized due to a manufacturing sterilization issue.",
      "recall_initiation_date": "20260731",
      "center_classification_date": "20260911",
      "report_date": "20260923",
      "code_info": "Catalog number: FLEXS-150-QFT; UDI-DI: 00616258022895; Affected material number: 87078825; Affected batch number: 8688750;",
      "more_code_info": ""
    }
  ]
}