{
  "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,
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    }
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  "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-1359-2025",
      "product_description": "OPEN HEART A PACK  , Model No UTOH19AI  UTOH19AJ-01  UTOH19AJ-02",
      "product_quantity": "54 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": "UDI-DI 00191072184450 00191072221070  Lots 921241 70-051173 70-052439"
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}