{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83218",
      "recalling_firm": "Clariance Inc",
      "address_1": "4809 N Ravenswood Ave Unit 119",
      "address_2": "N/A",
      "postal_code": "60640-4417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution to CA, IL, IN, NY, OH, TX.",
      "recall_number": "Z-1986-2019",
      "product_description": "Erisma- LP posterior fixation system with the below specifically affected products:      1. Erisma-LP polyaxial screws - 4.5, 5.5, 6.5, 7.5, 8.5, 9.5, 105 mm (all lengths);      2. Erisma-LP Screwdriver;      3. Erisma-LP T20 Wrench;      4. Erisma-LPT20 Snap Fit Tightening Wrench",
      "product_quantity": "4,090 units distributed in the US",
      "reason_for_recall": "Potential for the polyaxial screw to become disassembled during implant.",
      "recall_initiation_date": "20190701",
      "center_classification_date": "20190718",
      "termination_date": "20200709",
      "report_date": "20190724",
      "code_info": "1. Catalog Numbers: 181545XX, 181555XX, 181565XX, 181575XX, 181585XX, 181595XX, 181510XX;      2. Catalog Number 18710024;      3. Catalog Number 18720000;      4. Catalog Number 01720001"
    }
  ]
}