{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Peachtree Corners",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88656",
      "recalling_firm": "Stradis Medical, LLC dba Stradis Healthcare",
      "address_1": "3025 Northwoods Pkwy",
      "address_2": "N/A",
      "postal_code": "30071-1524",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed nationwide to VA, SC, CA, PA, MA, FL, TN, NJ, GA, AZ, IL, OH, OK, WA, NY, NV, MO, MD, IN, TX, CO, RI, NC, KY, MT, VI, GA, KS, MI, AK, ID, SD, UT and internationally to Canada.",
      "recall_number": "Z-0130-2022",
      "product_description": "Foundation Kit",
      "product_quantity": "790 kits",
      "reason_for_recall": "Firm unable to confirm that the tenaculum devices were produced in accordance with required design and manufacturing standards.",
      "recall_initiation_date": "20210910",
      "center_classification_date": "20211016",
      "report_date": "20211027",
      "code_info": "Part Number: A10"
    }
  ]
}