{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Mcminnville",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98987",
      "recalling_firm": "DT MedTech, LLC",
      "address_1": "111 Moffitt St",
      "address_2": "N/A",
      "postal_code": "37110-2235",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.",
      "recall_number": "Z-2399-2026",
      "product_description": "Hintermann Series Talar Implant, Left, Size 2  REF 302112",
      "product_quantity": "67 units",
      "reason_for_recall": "Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.",
      "recall_initiation_date": "20260324",
      "center_classification_date": "20260610",
      "report_date": "20260617",
      "code_info": "Lot: AACAA/ DI: B095302112"
    }
  ]
}