{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Roswell",
      "address_1": "1400 Holcomb Bridge Rd",
      "reason_for_recall": "Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.",
      "address_2": "",
      "product_quantity": "55 cases (10 units per case = 550 units)",
      "code_info": "Lot M3085K301 and M2327K301",
      "center_classification_date": "20140128",
      "distribution_pattern": "US Distribution in states of: AZ, CA, DE, FL, LA, MD, MA, NJ, NY, OH, PA and TX.",
      "state": "GA",
      "product_description": "Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Kimberly-Clark,Product code PMF22-100-10    The product is used to create lesions in nervous tissue when used with the Kimberly-Clark radiofrequency generator and probes.",
      "report_date": "20140205",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Kimberly-Clark Corporation",
      "recall_number": "Z-0850-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66832",
      "termination_date": "20140903",
      "more_code_info": "",
      "recall_initiation_date": "20131029",
      "postal_code": "30076-2190",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}