{
  "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": "Ongoing",
      "city": "Leesburg",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89522",
      "recalling_firm": "K2M, Inc",
      "address_1": "600 Hope Pkwy SE",
      "address_2": "",
      "postal_code": "20175-4428",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide.",
      "recall_number": "Z-0705-2022",
      "product_description": "Everest MI XT Inner Dilator, Catalog Number 5101-90167",
      "product_quantity": "686 Total Devices",
      "reason_for_recall": "Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting  together properly during a surgical procedure. Some dilators from these lots and from other lots were subsequently determined to be affected by a manufacturing nonconformance.",
      "recall_initiation_date": "20220113",
      "center_classification_date": "20220301",
      "report_date": "20220309",
      "code_info": "GTIN: 10888857261204; Lot Numbers: JUJF KFMV KUPG KYYU MDRB NDMK NDMX NXJK",
      "more_code_info": ""
    }
  ]
}