{
  "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
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  },
  "results": [
    {
      "country": "United States",
      "city": "Westlake Village",
      "address_1": "3050 E Hillcrest Dr",
      "reason_for_recall": "Issue with design specification; oversized condition.",
      "address_2": "",
      "product_quantity": "205",
      "code_info": "Lot #50174, 39799, 49364",
      "center_classification_date": "20160802",
      "distribution_pattern": "U.S. distribution to the following; CA, WA, UT, GA, AZ, NE, OR, MI, TX, WI, FL, AL, AR, MO, VA, MA, TN, LA, NC, KS, NY, SC, OK.    Foreign distribution to the following; CA, DE, IT, GB, PL, DE, GB, NL, GR, ES, HR, BG.",
      "state": "CA",
      "product_description": "RePlant¿ Angled Abutment  Part Number 6050-52-60",
      "report_date": "20160810",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Implant Direct Sybron Manufacturing, LLC",
      "recall_number": "Z-2320-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74624",
      "termination_date": "20170216",
      "more_code_info": "",
      "recall_initiation_date": "20160705",
      "postal_code": "91362-3171",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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  ]
}