{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88722",
      "recalling_firm": "DePuy Orthopaedics, Inc.",
      "address_1": "700 Orthopaedic Dr",
      "address_2": "",
      "postal_code": "46582-3994",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of CA, LA, MN, MO, NC, NE, OR, PA, WA, WI.",
      "recall_number": "Z-0074-2022",
      "product_description": "ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement  Part Code:152307001",
      "product_quantity": "10 units",
      "reason_for_recall": "Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery",
      "recall_initiation_date": "20210909",
      "center_classification_date": "20211007",
      "termination_date": "20230809",
      "report_date": "20211013",
      "code_info": "Lot Number: J6304Z GTIN: 10603295057642",
      "more_code_info": ""
    }
  ]
}