{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Cloud",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89412",
      "recalling_firm": "Microbiologics Inc",
      "address_1": "200 Cooper Ave N",
      "address_2": "N/A",
      "postal_code": "56303-4440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution in the countries of Canada and Germany.",
      "recall_number": "Z-0636-2022",
      "product_description": "KWIK-STIK(TM) labeled as containing Actinomyces odontolyticus.      Each KWIK-STIK\" unit contains a lyophilized pellet of a single microorganism strain, a reservoir of hydrating fluid and an inoculating swab. Each device is sealed within a laminated pouch that contains a desiccant to prevent adverse moisture accumulation. A KWIK-STIK\" catalog number ending in  P  is a duopak and contains two KWIKSTIK\" sticks.",
      "product_quantity": "2 units",
      "reason_for_recall": "Potential for product labeled as Actinomyces odontolyticus is actually Eggerthella lenta.",
      "recall_initiation_date": "20170302",
      "center_classification_date": "20220210",
      "termination_date": "20220422",
      "report_date": "20220216",
      "code_info": "Catalog Number: 0939P,  Lot Number: 939-47-2,  UDI: 20845357022701"
    }
  ]
}