{
  "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": "Saint Cloud",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97168",
      "recalling_firm": "Microbiologics Inc",
      "address_1": "200 Cooper Ave N",
      "address_2": "",
      "postal_code": "56303-4440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of France, Colombia, Philippines, Peru, Turkey, India, Finland, Trinidad and Tobago, Poland, Viet Nam, Brazil, Japan, Malaysia, Costa Rica.",
      "recall_number": "Z-2195-2025",
      "product_description": "LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as:  1) REF 0894L",
      "product_quantity": "",
      "reason_for_recall": "KWIK-STIK REF numbers:  0894P, 0894K and LYFO DISK\" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.",
      "recall_initiation_date": "20250627",
      "center_classification_date": "20250729",
      "report_date": "20250806",
      "code_info": "1) 0894L:  UDI/DI 10845357021967, Lot Numbers 894-76-4 and 894-76-6",
      "more_code_info": ""
    }
  ]
}