{
  "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": [
    {
      "status": "Terminated",
      "city": "Kennett Square",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69433",
      "recalling_firm": "Medartis, Inc.",
      "address_1": "127 W Street Rd Ste 203",
      "address_2": "N/A",
      "postal_code": "19348-1698",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of WV, IL, CT, AZ, and WA.",
      "recall_number": "Z-0150-2015",
      "product_description": "APTUS Ulna Shortening 2.5     Product Usage:  APTUS Ulna Shortening 2.5 Plates are indicated for fractures and osteotomies, in particular for the ulna.",
      "product_quantity": "44",
      "reason_for_recall": "A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to three (3) complaints of breakage of the temporary tension bolt.",
      "recall_initiation_date": "20141001",
      "center_classification_date": "20141030",
      "termination_date": "20150806",
      "report_date": "20141105",
      "code_info": "Part no. A-2791.05, lot no. 14125026",
      "more_code_info": ""
    }
  ]
}