{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Jacksonville",
      "address_1": "6743 Southpoint Dr N",
      "reason_for_recall": "Routine sterilization dose does not meet the required Sterility Assurance Level.",
      "address_2": "",
      "product_quantity": "29320 units",
      "code_info": "UDI: 20885074749024; SPONGE 2202-501EX LAMICEL 20PK 3MM INTL; 2202-501EX; Lots 9646605, 9651239, 9651240, 9651245, 9667694, 9667697, 9667756, 9669946, 9686127, 9686128, 9688076, 9693346, 9693347, 9693339, 9775264, 9799705, 9799708, 9811174, 9812616, 9819177, 9819513, 9819516, 9851438",
      "center_classification_date": "20191223",
      "distribution_pattern": "Affected product was only distributed in Japan.",
      "state": "FL",
      "product_description": "Lamicel 20PK 3MM INTL Cervical dilator",
      "report_date": "20200101",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Xomed, Inc.",
      "recall_number": "Z-0733-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84332",
      "more_code_info": "",
      "recall_initiation_date": "20191113",
      "postal_code": "32216-6218",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}