{
  "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
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Raleigh",
      "address_1": "6501 Six Forks Rd",
      "reason_for_recall": "Complaints reported of Radiesse (+) unable to be expelled from the syringe and/or needle.",
      "address_2": "",
      "product_quantity": "1,591 units",
      "code_info": "Model number: 8063M0K1, Lot #100088744.",
      "center_classification_date": "20160819",
      "distribution_pattern": "US Nationwide Distribution in the states of AR, CA, CO, CT, DC, FL, GA, IL, IN, LA, MA, MD, MI, MN, MO, NC, ND, NJ, NV, NY, OH, OK, OR, PA, PR, RI, SC, TN, TX, UT, VA, VT and WA.",
      "state": "NC",
      "product_description": "Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics.    Product Usage:  RADIESSE is indicated for sub-dermal implantation for the correction of moderate to severe facial wrinkles and folds.",
      "report_date": "20160831",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merz North America, Inc.",
      "recall_number": "Z-2607-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74252",
      "termination_date": "20170508",
      "more_code_info": "",
      "recall_initiation_date": "20160520",
      "postal_code": "27615-6515",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}