{
  "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": "307 packs; 6140 units",
      "code_info": "UDI: 20885074749055; SPONGE 2203-501EX LAMICEL 20PK 5MM INTL; 2203-501EX; Lots 9642542, 9657414, 9657415, 9657416, 9677915, 9707331, 9707338, 9707334, 9712918",
      "center_classification_date": "20191223",
      "distribution_pattern": "Affected product was only distributed in Japan.",
      "state": "FL",
      "product_description": "Lamicel 20PK 5MM INTL",
      "report_date": "20200101",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Xomed, Inc.",
      "recall_number": "Z-0734-2020",
      "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"
    }
  ]
}