{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bloomington",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90052",
      "recalling_firm": "Tornier, Inc",
      "address_1": "10801 Nesbitt Ave S",
      "address_2": "N/A",
      "postal_code": "55437-3109",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1216-2022",
      "product_description": "Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit",
      "product_quantity": "1066 units",
      "reason_for_recall": "The device is unable to meet sterilization requirements when sterilized per instructions in an Aesculap container.",
      "recall_initiation_date": "20220503",
      "center_classification_date": "20220601",
      "report_date": "20220608",
      "code_info": "Model: MWJ128, Ratcheting Screwdriver Handle, all lot codes"
    }
  ]
}