{
  "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": "Tiffin",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96343",
      "recalling_firm": "American Contract Systems Inc",
      "address_1": "85 Shaffer Park Dr",
      "address_2": "N/A",
      "postal_code": "44883-9290",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of OH.",
      "recall_number": "Z-1332-2025",
      "product_description": "DR DIULUS INJECTION PACK, Model Nos.   CCDU12C  CCDU12D  CCDU12D-01",
      "product_quantity": "1200 kits",
      "reason_for_recall": "ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.",
      "recall_initiation_date": "20250206",
      "center_classification_date": "20250314",
      "report_date": "20250326",
      "code_info": "1. Model No. CCDU12C UDI-DI 00191072196323 Tray Lots 968241 70-050508 70-050945 70-051497 70-051882  2. Model No. CCDU12D UDI-DI 00191072229472 Tray Lot 70-052444  3. Model No. CCDU12D-01 UDI-DI 00191072229472 Tray Lot 70-052967"
    }
  ]
}