{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Towson",
      "address_1": "110 West Rd Ste 227",
      "reason_for_recall": "Incorrect package labeling identifying the device",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "Lot: AAAEM",
      "center_classification_date": "20181107",
      "distribution_pattern": "Australia, Ireland, Korea, Germany",
      "state": "MD",
      "product_description": "DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE 4  Part Number: 302114 components are prostheses for a mobile bearing ankle joint.",
      "report_date": "20181114",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "DT MedTech, LLC",
      "recall_number": "Z-0403-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "81293",
      "termination_date": "20191205",
      "more_code_info": "",
      "recall_initiation_date": "20180925",
      "postal_code": "21204-2341",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}