{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "220366",
      "product_res_number": "Z-2399-2026",
      "event_date_initiated": "2026-03-24",
      "event_date_posted": "2026-06-10",
      "recall_status": "Open, Classified",
      "res_event_number": "98987",
      "product_code": "NTG",
      "pma_numbers": [
        "P160036"
      ],
      "product_description": "Hintermann Series Talar Implant, Left, Size 2\nREF 302112",
      "code_info": "Lot: AACAA/ DI: B095302112",
      "firm_fei_number": "3012104767",
      "recalling_firm": "DT MedTech, LLC",
      "address_1": "111 Moffitt St",
      "city": "Mcminnville",
      "state": "TN",
      "postal_code": "37110-2235",
      "additional_info_contact": "Customer Service\n1800-521-5002",
      "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.",
      "root_cause_description": "Labeling Change Control",
      "action": "On March 24, 2026,  DT MedTech issued a Urgent Medical Device Recall Notification to affected consignees.  DT MedTech requested that the firm take the following actions:\n\n1. Return of all available stock of Hintermann Series Talar Implants (Part/REF number 302112, Lot number AACAA)\n\n2. Please provide confirmation that all available stock of the part detailed below has been returned to Vilex LLC at 4516 S 700 E Suite 100A Salt Lake City, Utah 84107 USA.\n\n3. For any questions or concerns, contact Vilex Quality at quality@vilex.com or 800-521-5002.",
      "product_quantity": "67 units",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.",
      "openfda": {
        "pma_number": [
          "P160036",
          "P050050"
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        "device_name": "Prosthesis, Ankle, Uncemented, Non-Constrained",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
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