{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Ventura",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97703",
      "recalling_firm": "TMJ Solutions Inc",
      "address_1": "6059 King Dr",
      "address_2": "",
      "postal_code": "93003-7607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: IL, OR, MS, TX, OK, UT, MA, MD, NY, PA, VA, FL, CA, MN,  GA OUS: Canada, Spain, Brazil,",
      "recall_number": "Z-0488-2026",
      "product_description": "TMJ Bilateral Implant  REF: CHG020  Sterile EO, Rx Only",
      "product_quantity": "63 units",
      "reason_for_recall": "Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.",
      "recall_initiation_date": "20251013",
      "center_classification_date": "20251114",
      "report_date": "20251126",
      "code_info": "UDI: 07613327626551,07613327626568,07613327626575,07613327626605,07613327627749 07613327627848/ Lot #s: 2410301062 2306091054 2312121078 2401181023 2401231058 2403191046 2404291064 2405021079 2407221023 2407241032 2408081047 2408131037 2408161043 2409031033 2409241016 2410011097 2410071065 2410091014 2410111030 2410291062 2411111012 2411121044 2411201015 2412061031 2412121062 2412201009 2501021011",
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}