{
  "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": "Center Valley",
      "address_1": "3773 Corporate Pkwy",
      "reason_for_recall": "The trial insertion instrument may disassemble during use due to a potentially weak weld on then trial inserter shaft block area located near the thumb wheel.",
      "address_2": "",
      "product_quantity": "30",
      "code_info": "model no. ME020R",
      "center_classification_date": "20131119",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) GA, TN, CA, WY, NV, TX, OK, OH, and IL; and internationally to Canada.",
      "state": "PA",
      "product_description": "Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)",
      "report_date": "20131127",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Aesculap, Inc.",
      "recall_number": "Z-0361-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66534",
      "termination_date": "20141216",
      "more_code_info": "",
      "recall_initiation_date": "20130920",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}