{
  "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": [
    {
      "status": "Terminated",
      "city": "Fenton",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64931",
      "recalling_firm": "Progressive Medical Inc",
      "address_1": "997 Horan Dr",
      "address_2": "N/A",
      "postal_code": "63026-2401",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including AR, AZ, CA, CO, FL, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, NE, OH, OK, OR, TN, TX, WA, and WI.",
      "recall_number": "Z-1355-2013",
      "product_description": "Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -Laparoscopic Electrode PTFE Coated Curved Blade 33cm Length, Product number P0019 Rx Only.  Sterilized by Radiation.  Manufactured for Progressive Medical, Inc., St. Louis, MO 63128.      Electrodes used in Electrosurgeries",
      "product_quantity": "38 boxes with 6 units each.",
      "reason_for_recall": "Product coatings require 510K approval.",
      "recall_initiation_date": "20130412",
      "center_classification_date": "20130522",
      "termination_date": "20140507",
      "report_date": "20130529",
      "code_info": "Lot number 071212-04"
    }
  ]
}