{
  "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": "Cirencester",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90662",
      "recalling_firm": "Corin Ltd",
      "address_1": "Unit 1-57-8",
      "address_2": "Corinium Centre",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to NJ.  There was no military/government distribution.",
      "recall_number": "Z-1667-2022",
      "product_description": "TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800.  Orthopedic hip implant component.",
      "product_quantity": "1",
      "reason_for_recall": "Some of the devices did not pass fatigue testing.",
      "recall_initiation_date": "20220712",
      "center_classification_date": "20220831",
      "report_date": "20220907",
      "code_info": "Model #588.3800, Lot #494754; UDI 05055343871065",
      "more_code_info": ""
    }
  ]
}