{
  "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": "Union City",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90603",
      "recalling_firm": "Mizuho OSI",
      "address_1": "30031 Ahern Ave",
      "address_2": "",
      "postal_code": "94587-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S Nationwide Distribution .: CA, FL, GA, MI, NE, NJ, TN, UT, and WA    O.U.S.: Canada",
      "recall_number": "Z-1573-2022",
      "product_description": "HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144",
      "product_quantity": "13 devices",
      "reason_for_recall": "One batch of \"regular\" femoral hooks were incorrectly etched with the \"classic\" femoral hook model number.",
      "recall_initiation_date": "20210729",
      "center_classification_date": "20220824",
      "report_date": "20220831",
      "code_info": "Model Number: 6850-144  UDI Code: (01)00842430106842(10)MIZ210712(11)210712  Lot/Batch Number: MIZ210712",
      "more_code_info": ""
    }
  ]
}